Substituted (thioxo)carbonylaminophenyluracils

ABSTRACT

The invention relates to compounds of the formula (I) 
     
       
         
         
             
             
         
       
         
         
           
             in which Q, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7  are as defined in the disclosure, to processes for their preparation, and to their use as herbicides.

The present patent application has been filed under 35 U.S.C. 371 as anational stage application of PCT/EP03/04138, filed Apr. 22, 2003, whichwas published in German as International Patent Publication WO 03/093244on Nov. 13, 2003, which is entitled to the right of priority of GermanPatent Application 102 19 434.3, filed May 2, 2002.

The invention relates to novel substituted(thioxo)carbonylaminophenyluracils, to the process for their preparationand to their use as plant treatment agents, in particular as herbicides.

Certain substituted aryluracils are already known (for example EP-A-408382, U.S. Pat. Nos. 5,084,084, 5,127,935, 5,154,755, EP-A-563 384, U.S.Pat. No. 5,356,863, JP-A-09 048 761—cited in Chem. Abstracts 126:238387,WO 99/21837 A, U.S. Pat. No. 6,303,783). However, these compounds havehitherto not attained any particular importance since they have a numberof disadvantages.

This invention now provides novel substituted(thioxo)carbonylaminophenyluracils of the general formula (I)

in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or optionally cyano, halogen or    C₁-C₄-alkoxy-substituted alkyl having 1 to 6 carbon atoms,-   R² represents carboxyl, cyano, carbamoyl, thiocarbamoyl or in each    case optionally cyano, halogen or C₁-C₄-alkoxy-substituted alkyl or    alkoxy-carbonyl having in each case 1 to 6 carbon atoms in the alkyl    groups,-   R³ represents hydrogen, halogen or optionally halogen-substituted    alkyl having 1 to 6 carbon atoms,-   R⁴ represents hydrogen, cyano, carbamoyl, thiocarbamoyl or halogen,-   R⁵ represents cyano, carbamoyl, thiocarbamoyl, halogen, or    represents in each case optionally halogen-substituted alkyl or    alkoxy having in each case 1 to 6 carbon atoms,-   R⁶ represents hydrogen, represents optionally cyano-, carboxyl-,    halogen-, C₁-C₄-alkoxy-, C₁-C₄-alkylthio-, C₁-C₄-alkylsulphinyl-,    C₁-C₄-alkylsulphonyl-, C₁-C₄-alkyl-carbonyl- or    C₁-C₄-alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms,    represents in each case optionally cyano-, halogen- or    C₁-C₄-alkoxy-substituted alkylcarbonyl, alkoxycarbonyl or    alkylsulphonyl having in each case 1 to 6 carbon atoms in the alkyl    groups, represents in each case optionally halogen-substituted    alkenyl, alkenylcarbonyl, alkenylsulphonyl or alkynyl having in each    case 3 to 6 carbon atoms in the alkenyl or alkynyl groups,    represents in each case optionally cyano, halogen or    C₁-C₄-alkyl-substituted cycloalkyl, cycloalkylalkyl,    cycloalkylcarbonyl, cycloalkylalkylcarbonyl, cycloalkylsulphonyl or    cycloalkylalkylsulphonyl having in each case 3 to 6 carbon atoms in    the cycloalkyl groups and, if appropriate, 1 to 4 carbon atoms in    the alkyl moiety, represents in each case optionally nitro-, cyano-,    halogen-, C₁-C₄-alkyl-, C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-,    C₁-C₄-haloalkoxy- or C₁-C₄-alkoxy-carbonyl-substituted aryl,    arylalkyl, arylcarbonyl, arylalkylcarbonyl, arylsulphonyl or    arylalkylsulphonyl having in each case 6 or 10 carbon atoms in the    aryl groups and, if appropriate, 1 to 4 carbon atoms in the alkyl    moiety, or represents in each case optionally nitro-, cyano-,    halogen-, C₁-C₄-alkyl-, C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-,    C₁-C₄-haloalkoxy- or C₁-C₄-alkoxy-carbonyl-substituted    heterocyclylcarbonyl, heterocyclylalkylcarbonyl,    heterocyclylsulphonyl or heterocyclylalkylsulphonyl having in each    case up to 6 carbon atoms, up to 5 nitrogen atoms and/or 1 or 2    oxygen or sulphur atoms as ring members—where the heterocyclyl    groups in each case also optionally contain 1 or 2 —SO groups, 1 or    2 —SO₂ groups, 1 or 2 —CO groups or 1 or 2 —CS groups, and-   R⁷ represents in each case optionally halogen-substituted    alkoxycarbonylalkoxy, alkoxycarbonylalkylthio,    alkenyloxycarbonylalkoxy, alkenyloxycarbonylalkylthio,    alkynyloxycarbonylalkoxy, alkynyloxycarbonylalkylthio,    carbamoylalkoxy, carbamoylalkylthio, alkylaminocarbonylalkoxy,    alkylaminocarbonylalkylthio, dialkylaminocarbonylalkoxy,    dialkylaminocarbonylalkylthio, N-alkyl-N-alkenylaminocarbonylalkoxy,    N-alkyl-N-alkenylaminocarbonylalkylthio,    dialkenylaminocarbonylalkoxy, dialkenylaminocarbonylalkylthio,    N-alkyl-N-alkynylaminocarbonylalkoxy,    N-alkyl-N-alkynylaminocarbonylalkylthio having in each case up to 6    carbon atoms in the alkyl, alkenyl or alkynyl groups, or-   R⁷ represents hydroxyamino, represents in each case optionally    halogen-substituted N-alkylhydroxyamino, alkoxyamino,    N-alkylalkoxyamino, alkoxycarbonylalkoxyamino or    N-alkylalkoxycarbonylalkoxyamino having in each case 1 to 6 carbon    atoms in the alkyl groups, represents in each case optionally    halogen-substituted alkenyloxyamino, N-alkylalkenyloxyamino,    N-alkenylalkoxyamino or N-alkenylalkenyloxyamino having in each case    3 to 6 carbon atoms in the alkenyl groups and, if appropriate, 1 to    6 carbon atoms in the alkyl groups, represents cycloalkyloxyamino or    N-alkylcycloalkyloxyamino having in each case 3 to 6 carbon atoms in    the cycloalkyl groups and, if appropriate, 1 to 6 carbon atoms in    the alkyl group, or represents in each case optionally    halogen-substituted aryloxyamino or N-alkylaryloxyamino having in    each case 6 or 10 carbon atoms in the aryl groups and, if    appropriate, 1 to 6 carbon atoms in the alkyl group, or-   R⁷ represents cyanoalkylamino having 1 to 6 carbon atoms, represents    optionally cyano-, halogen-, C₁-C₄-alkoxy- or    C₁-C₄-alkoxycarbonyl-substituted dialkylamino having in each case 1    to 6 carbon atoms in the alkyl groups, represents in each case    optionally cyano-, halogen- or C₁-C₄-alkoxy-carbonyl-substituted    N-alkyl-N-alkenylamino or N-alkyl-N-alkynylamino having in each case    up to 6 carbon atoms in the alkyl, alkenyl or alkynyl groups, or    represents dialkenylamino or dialkynylamino having in each case up    to 6 carbon atoms in the alkenyl or alkynyl groups, or-   R⁷ represents in each case optionally nitro-, cyano-, halogen-,    C₁-C₄-alkyl-, C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-, C₁-C₄-haloalkoxy-,    C₁-C₄-alkylthio-, C₁-C₄-haloalkylthio-, C₁-C₄-alkoxy-carbonyl-,    C₃-C₆-cycloalkyl- or phenyl-substituted heterocyclyloxy,    heterocyclylthio, heterocyclylamino, N-alkylheterocyclylamino,    N-alkylheterocyclylalkylamino or —N=(heterocyclyl), where the    monocyclic or bicyclic heterocyclyl group contains up to 6 carbon    atoms, up to 5 nitrogen atoms and/or 1 or 2 oxygen atoms and/or 1 or    2 sulphur atoms and optionally additionally 1 or 2 —SO groups and/or    1 or 2 —SO₂ groups and/or 1 or 2 —CO groups and/or 1 or 2 —CS    groups, and the alkyl group contains, if appropriate, 1 to 6 carbon    atoms, or-   R⁷ represents a monocyclic or bicyclic nitrogen heterocycle which is    attached via N, contains up to 9 carbon atoms, up to 5 nitrogen    atoms and optionally additionally 1 or 2 oxygen or sulphur atoms and    optionally additionally 1 or 2 —SO groups, 1 or 2 —SO₂ groups, 1 or    2 —CO groups, 1 or 2 —CS groups or one cyanoimino group (C═N—CN) and    is optionally substituted by nitro, cyano, halogen, C₁-C₄-alkyl,    C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio,    C₁-C₄-haloalkylthio, C₁-C₄-alkoxy-carbonyl,    C₁-C₄-alkoxy-carbonyl-C₁-C₂-alkoxy, C₁-C₄-alkyl-carbonylamino,    C₁-C₄-alkoxy-carbonyl-amino, C₂-C₄-alkylenedioxy, C₃-C₆-cycloalkyl    or phenyl,    including the possible stereoisomeric forms.

In the definitions, the hydrocarbon chains, such as alkyl or alkenyl,are in each case straight-chain or branched—including in combinationwith heteroatoms, such as in alkoxy.

Optionally substituted radicals can be mono- or polysubstituted, wherein the case of polysubstitution the substituents can be identical ordifferent.

Preferred substituents or ranges of radicals present in the formulaelisted above and below are defined below:

-   Q preferably represents oxygen.-   R¹ preferably represents hydrogen, amino or optionally cyano-,    fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or    i-propoxy-substituted alkyl having 1 to 5 carbon atoms.-   R² preferably represents carboxyl, cyano, carbamoyl, thiocarbamoyl    or in each case optionally cyano-, fluorine-, chlorine-, bromine-,    methoxy-, ethoxy-, n- or i-propoxy-substituted alkyl or    alkoxycarbonyl having in each case 1 to 5 carbon atoms in the alkyl    groups.

R³ preferably represents hydrogen, fluorine, chlorine, bromine oroptionally fluorine-, chlorine- or bromine-substituted alkyl having 1 to5 carbon atoms.

-   R⁴ preferably represents hydrogen, cyano, carbamoyl, thiocarbamoyl,    fluorine, chlorine or bromine.-   R⁵ preferably represents cyano, carbamoyl, thiocarbamoyl, fluorine,    chlorine, bromine, or in each case optionally fluorine-, chlorine-    or bromine-substituted alkyl or alkoxy having in each case 1 to 5    carbon atoms.-   R⁶ preferably represents hydrogen, represents optionally cyano-,    carboxyl-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or    i-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-,    methylsulphinyl-, ethylsulphinyl-, n- or i-propylsulphinyl-,    methylsulphonyl- or ethylsulphonyl-, acetyl-, propionyl-, n- or    i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted alkyl having 1 to 5 carbon atoms,    represents in each case optionally cyano-, fluorine-, chlorine-,    bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted    alkylcarbonyl, alkoxycarbonyl or alkylsulphonyl having in each case    1 to 5 carbon atoms in the alkyl groups, represents in each case    optionally fluorine-, chlorine- or bromine-substituted alkenyl,    alkenyl-carbonyl, alkenylsulphonyl or alkynyl having in each case 3    to 5 carbon atoms in the alkenyl or alkynyl groups, represents in    each case optionally cyano-, fluorine-, chlorine-, bromine-,    methyl-, ethyl-, n- or i-propyl-substituted cycloalkyl,    cycloalkylalkyl, cycloalkylcarbonyl, cycloalkylalkylcarbonyl,    cycloalkylsulphonyl or cycloalkylalkylsulphonyl having in each case    3 to 6 carbon atoms in the cycloalkyl groups and, if appropriate, 1    to 3 carbon atoms in the alkyl moiety, represents in each case    optionally nitro-, cyano-, fluorine-, chlorine-, bromine-, methyl-,    ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-,    chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n-    or i-propoxy-, n-, i-, s- or t-butoxy-, difluoromethoxy-,    trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,    methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-,    s- or t-butoxycarbonyl-substituted aryl, arylalkyl, arylcarbonyl,    arylalkylcarbonyl, arylsulphonyl or arylalkylsulphonyl having in    each case 6 or 10 carbon atoms in the aryl groups and, if    appropriate, 1 to 3 carbon atoms in the alkyl moiety, or represents    in each case optionally nitro-, cyano-, fluorine-, chlorine-,    bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-,    trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,    methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-, n-, i-, s- or t-butoxycarbonyl-substituted    heterocyclylcarbonyl, heterocyclylalkylcarbonyl,    heterocyclylsulphonyl or heterocyclylalkylsulphonyl having in each    case up to 5 carbon atoms, up to 4 nitrogen atoms and/or one oxygen    or sulphur atom as ring members—where the heterocyclyl groups each    also optionally contain an —SO group, an —SO₂ group, 1 or 2 —CO    groups or 1 or 2 —CS groups.-   R⁷ preferably represents in each case optionally halogen-substituted    alkoxycarbonylalkoxy, alkoxycarbonylalkylthio,    alkenyloxycarbonylalkoxy, alkenyloxycarbonylalkylthio,    alkynyloxycarbonylalkoxy, alkynyloxycarbonylalkylthio,    carbamoylalkoxy, carbamoylalkylthio, alkylaminocarbonylalkoxy,    alkylaminocarbonylalkylthio, dialkylaminocarbonylalkoxy,    dialkylaminocarbonylalkylthio, dialkenylaminocarbonylalkoxy,    dialkenylaminocarbonylalkylthio, dialkynylaminocarbonyloxy or    dialkynylaminocarbonylalkylthio having in each case up to 5 carbon    atoms in the alkyl, alkenyl or alkynyl groups.-   R⁷ furthermore preferably represents hydroxyamino, represents in    each case optionally halogen-substituted N-alkylhydroxyamino,    alkoxyamino, N-alkylalkoxyamino, alkoxycarbonylalkoxyamino or    N-alkylalkoxycarbonylalkoxyamino having in each case 1 to 5 carbon    atoms in the alkyl groups, represents in each case optionally    halogen-substituted alkenyloxyamino, N-alkylalkenyloxyamino,    N-alkenylalkoxyamino or N-alkenylalkenyloxyamino having in each case    3 to 5 carbon atoms in the alkenyl groups and, if appropriate, 1 to    5 carbon atoms in the alkyl groups, represents cycloalkyloxyamino or    N-alkylcycloalkyloxyamino having in each case 3 to 6 carbon atoms in    the cycloalkyl groups and, if appropriate, 1 to 3 carbon atoms in    the alkyl group, or represents in each case optionally    halogen-substituted aryloxyamino or N-alkylaryloxyamino having in    each case 6 or 10 carbon atoms in the aryl groups and, if    appropriate, 1 to 3 carbon atoms in the alkyl group.-   R⁷ furthermore preferably represents cyanoalkylamino having 1 to 5    carbon atoms, represents in each case optionally cyano-, fluorine-,    chlorine-, methoxy-, ethoxy-, n- or i-propoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-substituted dialkylamino    having in each case 1 to 5 carbon atoms in the alkyl groups,    represents in each case optionally cyano-, fluorine-, chlorine-,    methoxy-, ethoxy-, n- or i-propoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-substituted    N-alkyl-N-alkenylamino or N-alkyl-N-alkynylamino having in each case    up to 5 carbon atoms in the alkyl, alkenyl or alkynyl groups,    represents dialkenylamino or dialkynylamino having in each case up    to 5 carbon atoms in the alkenyl or alkynyl groups.-   R⁷ furthermore preferably represents in each case optionally nitro-,    cyano-, fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or    i-propyl-, n-, i-, s- or t-butyl-, difluoromethyl-, dichloromethyl-,    trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,    methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s- or    t-butylthio-, difluoromethylthio-, trifluoromethylthio-,    chlorodifluoromethylthio-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-, n-, i-, s- or t-butoxycarbonyl-, cyclopropyl-,    cyclobutyl-, cyclopentyl-, cyclohexyl- or phenyl-substituted    heterocyclyloxy, heterocyclylthio, heterocyclylamino,    N-alkylheterocyclylamino, N-alkylheterocyclylalkylamino or    —N=(heterocyclyl), where the monocyclic or bicyclic heterocyclyl    group contains up to 6 carbon atoms, up to 5 nitrogen atoms and/or 1    or 2 oxygen atoms and/or 1 or 2 sulphur atoms and optionally    additionally 1 or 2 —SO groups and/or 1 or 2 —SO₂ groups and/or 1 or    2 —CO groups and/or 1 or 2 —CS groups and the alkyl group contains,    if appropriate, 1 to 3 carbon atoms.-   R⁷ furthermore preferably represents a monocyclic or bicyclic    nitrogen heterocycle which is attached via N, contains up to 9    carbon atoms, up to 5 nitrogen atoms and optionally additionally 1    or 2 oxygen or sulphur atoms and optionally additionally 1 or 2 —SO    groups, 1 or 2 —SO2 groups, 1 or 2 —CO groups, 1 or 2 —CS groups or    one cyanoimino group (C═N—CN) and is optionally substituted by    nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or    i-propyl, n-, i-, s- or t-butyl, difluoromethyl, dichloromethyl,    trifluoromethyl, chlorodifluoromethyl, fluorodichloromethyl,    methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy,    difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy,    methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or    t-butylthio, difluoromethylthio, trifluoromethylthio,    chlorodifluoromethylthio, methoxycarbonyl, ethoxycarbonyl, n- or    i-propoxycarbonyl, n-, i-, s- or t-butoxycarbonyl,    methoxycarbonylmethoxy, ethoxycarbonylmethoxy, acetylamino,    propionylamino, methoxycarbonylamino, ethoxycarbonylamino,    ethylenedioxy, propylenedioxy, cyclopropyl, cyclobutyl, cyclopentyl,    cyclohexyl or phenyl.-   R¹ particularly preferably represents hydrogen, amino or in each    case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,    ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl,    n-, i- or s-butyl.-   R² particularly preferably represents carboxyl, cyano, carbamoyl,    thiocarbamoyl or in each case optionally cyano-, fluorine-,    chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted    methyl, ethyl, n- or i-propyl, methoxycarbonyl, ethoxycarbonyl, n-    or i-propoxycarbonyl.-   R³ particularly preferably represents hydrogen, fluorine, chlorine,    bromine or in each case optionally fluorine-, chlorine- or    bromine-substituted methyl, ethyl, n- or i-propyl.-   R⁴ particularly preferably represents hydrogen, cyano, carbamoyl,    thiocarbamoyl, fluorine, chlorine or bromine.-   R⁵ particularly preferably represents cyano, carbamoyl,    thiocarbamoyl, fluorine, chlorine, bromine, or in each case    optionally fluorine-, chlorine- or bromine-substituted methyl,    ethyl, n- or i-propyl, methoxy, ethoxy, n- or i-propoxy.-   R⁶ particularly preferably represents hydrogen, represents in each    case optionally cyano-, carboxyl-, fluorine-, chlorine-, bromine-,    methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, n- or    i-propylthio-, methylsulphinyl-, ethylsulphinyl-, n- or    i-propylsulphinyl-, methylsulphonyl- or ethylsulphonyl-, acetyl-,    propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n-    or i-propoxycarbonyl-substituted methyl, ethyl, n- or i-propyl, n-,    i- or s-butyl, represents in each case optionally cyano-, fluorine-,    chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted    acetyl, propionyl, n- or i-butyroyl, methoxycarbonyl,    ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s- or    t-butoxycarbonyl, methylsulphonyl, ethylsulphonyl, n- or    i-propylsulphonyl, n-, i- or s-butylsulphonyl, represents in each    case optionally fluorine-, chlorine- or bromine-substituted    propenyl, butenyl, propenylsulphonyl, butenylsulphonyl, propynyl or    butynyl, represents in each case optionally cyano-, fluorine-,    chlorine-, bromine-, methyl- or ethyl-substituted cyclopropyl,    cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylmethyl,    cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl,    cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl,    cyclohexylcarbonyl, cyclopropylmethylcarbonyl,    cyclobutylmethylcarbonyl, cyclopentylmethylcarbonyl,    cyclohexylmethylcarbonyl, cyclopropylsulphonyl, cyclobutylsulphonyl,    cyclopentylsulphonyl, cyclohexylsulphonyl,    cyclopropylmethylsulphonyl, cyclobutylmethylsulphonyl,    cyclopentylmethylsulphonyl or cyclohexylmethylsulphonyl, represents    in each case optionally nitro-, cyano-, fluorine-, chlorine-,    bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-,    trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,    methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-, n-, i-, s- or t-butoxycarbonyl-substituted    phenyl, phenylmethyl, phenylethyl, phenylpropyl, benzoyl,    phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl.-   R⁷ particularly preferably represents methoxycarbonylmethoxy,    ethoxycarbonylmethoxy, n- or i-propoxycarbonylmethoxy, n-, i-, s- or    t-butoxycarbonylmethoxy, methoxycarbonylethoxy,    ethoxycarbonylethoxy, n- or i-propoxycarbonylethoxy, n-, i-, s- or    t-butoxycarbonylethoxy, methoxycarbonylmethylthio,    ethoxycarbonylmethylthio, n- or i-propoxycarbonylmethylthio, n-, i-,    s- or t-butoxycarbonylmethylthio, methoxycarbonylethylthio,    ethoxycarbonylethylthio, n- or i-propoxycarbonylethylthio, n-, i-,    s- or t-butoxycarbonylethylthio, propenyloxycarbonylmethoxy,    butenyloxycarbonylmethoxy, propenyloxycarbonylethoxy,    butenyloxycarbonylethoxy, propenyloxycarbonylmethylthio,    butenyloxycarbonylmethylthio, propenyloxycarbonylethylthio,    butenyloxycarbonylethylthio, propynyloxycarbonylmethoxy,    butynyloxycarbonylmethoxy, propynyloxycarbonylethoxy,    butynyloxycarbonylethoxy, propynyloxycarbonylmethylthio,    butynyloxycarbonylmethylthio, propynyloxycarbonylethylthio,    butynyloxycarbonylethylthio, carbamoylmethoxy, carbamoylethoxy,    carbamoylmethylthio, carbamoylethylthio, methylaminocarbonylmethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylmethoxy, n-,    i-, s- or t-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-,    s- or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,    ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio,    n-, i-, s- or t-butylaminocarbonylmethylthio,    methylaminocarbonylethylthio, ethylaminocarbonylethylthio, n- or    i-propylaminocarbonylethylthio, n-, i-, s- or    t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,    diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,    diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,    diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,    diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,    dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,    dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,    dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio or    dipropynylaminocarbonylethylthio.-   R⁷ furthermore particularly preferably represents hydroxyamino,    represents N-methylhydroxyamino, N-ethylhydroxyamino,    N-n-propylhydroxyamino, N-i-propylhydroxyamino, methoxyamino,    ethoxyamino, n- or i-propoxyamino, n-, i-, s- or t-butoxyamino,    N-methylmethoxyamino, N-ethylmethoxyamino, N-methylethoxyamino,    methoxycarbonylmethoxyamino, ethoxycarbonylmethoxyamino, n- or    i-propoxycarbonylmethoxyamino, methoxycarbonylethoxyamino,    ethoxycarbonylethoxyamino, n- or i-propoxycarbonylethoxyamino,    N-methylmethoxycarbonylmethoxyamino,    N-methylethoxycarbonylmethoxyamino,    N-methyl-n-propoxycarbonylmethoxyamino,    N-methyl-i-propoxycarbonylmethoxyamino,    N-methylmethoxycarbonylethoxyamino,    N-methylethoxycarbonylethoxyamino,    N-methyl-n-propoxycarbonylethoxyamino,    N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,    butenyloxyamino, N-methylpropenyloxyamino, N-methylbutenyloxyamino,    N-propenyl-methoxyamino, N-propenylethoxyamino,    N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino,    N-propenylpropenyloxyamino, represents cyclopentyloxyamino,    cyclohexyloxyamino, N-methylcyclopentyloxyamino or    N-methylcyclohexyloxyamino, or represents phenoxyamino or    N-methylphenoxyamino.-   R⁷ furthermore particularly preferably represents cyanomethylamino,    cyanoethylamino, cyanopropylamino or cyanobutylamino, represents in    each case optionally cyano-, fluorine-, chlorine-, methoxy-,    ethoxy-, n- or i-propoxy-, methoxycarbonyl-, ethoxycarbonyl, n- or    i-propoxycarbonyl-substituted dimethylamino, diethylamino,    dipropylamino or dibutylamino, represents in each case optionally    cyano-, fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-,    methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted N-methyl-N-propenylamino,    N-methyl-N-butenylamino, N-ethyl-N-propenylamino,    N-ethyl-N-butenylamino, N-propyl-N-propenylamino,    N-propyl-N-butenylamino, N-butyl-N-propenylamino,    N-butyl-N-butenylamino, N-methyl-N-propynylamino,    N-methyl-N-butynylamino, N-ethyl-N-propynylamino,    N-ethyl-N-butynylamino, N-propyl-N-propynylamino,    N-propyl-N-butynylamino, N-butyl-N-propynylamino,    N-butyl-N-butynylamino, or represents dipropenylamino,    dibutenylamino, dipropynylamino or dibutynylamino.-   R⁷ furthermore particularly preferably represents in each case    optionally nitro-, cyano-, fluorine-, chlorine-, bromine-, methyl-,    ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, difluoromethyl-,    dichloromethyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, methylthio-, ethylthio-, n- or    i-propylthio-, n-, i-, s- or t-butylthio-, difluoromethylthio-,    trifluoromethylthio-, chlorodifluoromethylthio-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-, methoxycarbonylmethoxy-, acetylamino-,    ethylenedioxy-, propylenedioxy-, cyclopropyl-, cyclobutyl-,    cyclopentyl-, cyclohexyl- or phenyl-substituted heterocyclyloxy,    heterocyclylthio, heterocyclylamino, N-methylheterocyclylamino,    N-ethylheterocyclylamino, N-methylheterocyclylmethylamino,    N-ethylheterocyclylmethylamino or —N=(heterocyclyl), where the    heterocyclyl grouping is selected from the group consisting of    furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl,    oxopyrrolidinyl, pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl,    oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl, thiazolidinyl,    cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,    2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,    oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,    oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl,    pyrimidinyl.-   R⁷ furthermore particularly preferably represents a monocyclic or    bicyclic nitrogen heterocycle from the group consisting of pyrrolyl,    pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrazolyl, imidazolyl,    imidazolinyl, 2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl),    2-oxooxazolidinyl, isoxazolidinyl, thiazolinyl, 2-oxothiazolidinyl,    isothiazolidinyl, 1-oxoisothiazolidinyl, 1,1-dioxoisothiazolidinyl,    2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl,    thioxotriazolinyl, pyridinyl, piperidinyl, oxopiperidinyl,    1,2-oxazacyclohexyl, 1,2-oxazacyclohexenyl,    2-oxo-1,3-diazacyclohexyl, morpholinyl or piperazinyl, which is    attached via N and is optionally substituted by nitro, cyano,    fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-,    s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl,    chlorodifluoromethyl, fluorodichloromethyl, methoxy, ethoxy, n- or    i-propoxy, n-, i-, s- or t-butoxy, difluoromethoxy,    trifluoromethoxy, chlorodifluoromethoxy, methylthio, ethylthio, n-    or i-propylthio, n-, i-, s- or t-butylthio, difluoromethylthio,    trifluoromethylthio, chlorodifluoromethylthio, methoxycarbonyl,    ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s- or    t-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl    or phenyl.-   R¹ very particularly preferably represents hydrogen, amino or in    each case optionally cyano-, fluorine-, chlorine-, methoxy- or    ethoxy-substituted methyl, ethyl, n- or i-propyl.-   R² very particularly preferably represents in each case optionally    cyano-, fluorine-, chlorine-, methoxy-, ethoxy-, n- or    i-propoxy-substituted methyl, ethyl, n- or i-propyl.-   R³ very particularly preferably represents hydrogen, fluorine,    chlorine or in each case optionally fluorine- or    chlorine-substituted methyl or ethyl.-   R⁴ very particularly preferably represents hydrogen, fluorine or    chlorine.-   R⁵ very particularly preferably represents cyano, carbamoyl,    thiocarbamoyl, fluorine, chlorine, bromine, or in each case    optionally fluorine- or chlorine-substituted methyl, ethyl, methoxy    or ethoxy.-   R⁶ very particularly preferably represents hydrogen, represents in    each case optionally cyano-, carboxyl-, fluorine-, chlorine-,    methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl- or    ethylsulphonyl-, acetyl-, propionyl-, n- or i-butyroyl-,    methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted methyl, ethyl, n- or i-propyl, n-, i-    or s-butyl, represents in each case optionally cyano-, fluorine-,    chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted    acetyl, propionyl, n- or i-butyroyl, methoxycarbonyl,    ethoxycarbonyl, n- or i-propoxycarbonyl, methylsulphonyl,    ethylsulphonyl, n- or i-propylsulphonyl, n-, i- or s-butylsulphonyl,    represents in each case optionally fluorine-, chlorine- or    bromine-substituted propenyl, butenyl, propynyl or butynyl,    represents in each case optionally cyano-, fluorine-, chlorine-,    methyl- or ethyl-substituted cyclopropyl, cyclopentyl, cyclohexyl,    cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl,    cyclopropylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl,    cyclopropylsulphonyl, cyclopentylsulphonyl or cyclohexylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-, n-, i-, s- or t-butoxycarbonyl-substituted    phenyl, phenylmethyl, phenylethyl, benzoyl, phenylacetyl,    phenylsulphonyl or phenylmethylsulphonyl, or represents in each case    optionally nitro-, cyano-, fluorine-, chlorine-, bromine-, methyl-,    ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-,    chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n-    or i-propoxy-, n-, i-, s- or t-butoxy-, difluoromethoxy-,    trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,    methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-,    s- or t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl.-   R⁷ very particularly preferably represents methoxycarbonylmethoxy,    ethoxycarbonylmethoxy, n- or i-propoxycarbonylmethoxy, n-, i-, s- or    t-butoxycarbonylmethoxy, methoxycarbonylethoxy,    ethoxycarbonylethoxy, n- or i-propoxycarbonylethoxy, n-, i-, s- or    t-butoxycarbonylethoxy, methoxycarbonylmethylthio,    ethoxycarbonylmethylthio, n- or i-propoxycarbonylmethylthio, n-, i-,    s- or t-butoxycarbonylmethylthio, methoxycarbonylethylthio,    ethoxycarbonylethylthio, n- or i-propoxycarbonylethylthio, n-, i-,    s- or t-butoxycarbonylethylthio, propenyloxycarbonylmethoxy,    butenyloxycarbonylmethoxy, propenyloxycarbonylethoxy,    butenyloxycarbonylethoxy, propenyloxycarbonylmethylthio,    butenyloxycarbonylmethylthio, propenyloxycarbonylethylthio,    butenyloxycarbonylethylthio, propynyloxycarbonylmethoxy,    butynyloxycarbonylmethoxy, propynyloxycarbonylethoxy,    butynyloxycarbonylethoxy, propynyloxycarbonylmethylthio,    butynyloxycarbonylmethylthio, propynyloxycarbonylethylthio,    butynyloxycarbonylethylthio, methylaminocarbonylmethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylmethoxy, n-,    i-, s- or t-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-,    s- or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,    ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio,    n-, i-, s- or t-butylaminocarbonylmethylthio,    methylaminocarbonylethylthio, ethylaminocarbonylethylthio, n- or    i-propylaminocarbonylethylthio, n-, i-, s- or    t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,    diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,    diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,    diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,    diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,    dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,    dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,    dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio or    dipropynylaminocarbonylethylthio.-   R⁷ furthermore very particularly preferably represents hydroxyamino,    represents N-methylhydroxyamino, N-ethyl-hydroxyamino,    N-n-propylhydroxyamino, N-i-propylhydroxyamino, methoxyamino,    ethoxyamino, n- or i-propoxyamino, n-, i-, s- or t-butoxyamino,    N-methylmethoxyamino, N-ethylmethoxyamino, N-methylethoxyamino,    methoxycarbonylmethoxyamino, ethoxycarbonylmethoxyamino, n- or    i-propoxycarbonylmethoxyamino, methoxycarbonylethoxyamino,    ethoxycarbonylethoxyamino, n- or i-propoxycarbonylethoxyamino,    N-methylmethoxycarbonylmethoxyamino,    N-methylethoxycarbonylmethoxyamino,    N-methyl-n-propoxycarbonylmethoxyamino,    N-methyl-i-propoxycarbonylmethoxyamino,    N-methyl-methoxycarbonylethoxyamino,    N-methylethoxycarbonylethoxyamino,    N-methyl-n-propoxycarbonylethoxyamino,    N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,    butenyloxyamino, N-methyl-propenyloxyamino, N-methylbutenyloxyamino,    N-propenylmethoxyamino, N-propenylethoxyamino,    N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino,    N-propenylpropenyloxyamino, or represents phenoxyamino or    N-methylphenoxyamino.-   R⁷ furthermore very particularly preferably represents    cyanoethylamino, cyanopropylamino or cyanobutylamino, represents    dimethylamino, diethylamino, di-n-propylamino, di-i-propylamino,    di-n-butylamino or di-i-butylamino, represents    N-methylcyanoethylamino, N-ethylcyanoethylamino,    N-n-propylcyanoethylamino, N-i-propylcyanoethylamino,    N-methylfluoroethylamino, N-ethylfluoroethylamino,    N-n-propylfluoroethylamino, N-i-propylfluoroethylamino,    N-methylmethoxyethylamino, N-ethylmethoxyethylamino,    N-methylethoxyethylamino, N-ethylethoxyethylamino,    N-methylmethoxycarbonylmethylamino,    N-methylethoxycarbonylmethylamino,    N-methylmethoxycarbonylethylamino, N-methylethoxycarbonylethylamino,    represents N-methyl-N-propenylamino, N-methyl-N-butenylamino,    N-ethyl-N-propenylamino, N-ethyl-N-butenylamino,    N-propyl-N-propenylamino, N-propyl-N-butenylamino,    N-butyl-N-propenylamino, N-butyl-N-butenylamino,    N-methyl-N-propynylamino, N-methyl-N-butynylamino,    N-ethyl-N-propynylamino, N-ethyl-N-butynylamino,    N-propyl-N-propynylamino, N-propyl-N-butynylamino,    N-butyl-N-propynylamino or N-butyl-N-butynylamino, or represents    dipropenylamino, dibutenylamino, dipropynylamino or dibutynylamino.-   R⁷ furthermore very particularly preferably represents in each case    optionally nitro-, cyano-, fluorine-, chlorine-, bromine-, methyl-,    ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, difluoromethyl-,    dichloromethyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, methylthio-, ethylthio-, n- or    i-propylthio-, n-, i-, s- or t-butylthio-, difluoromethylthio-,    trifluoromethylthio-, chlorodifluoromethylthio-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-, cyclopropyl-, cyclobutyl-, cyclopentyl-,    cyclohexyl- or phenyl-substituted heterocyclyloxy, heterocyclylthio,    heterocyclylamino, N-methylheterocyclylamino,    N-methylheterocyclylmethylamino or —N=(heterocyclyl), where the    heterocyclyl grouping is selected from the group consisting of    furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl,    oxopyrrolidinyl, pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl,    oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl, thiazolidinyl,    cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,    2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,    oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,    oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl,    pyrimidinyl.-   R⁷ furthermore very particularly preferably represents a monocyclic    or bicyclic nitrogen heterocycle from the group consisting of    pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrazolyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), 2-oxo-1,3-oxazacyclopentyl    (2-oxooxazolidinyl), isoxazolidinyl, thiazolinyl,    2-oxothiazolidinyl, 1,1-dioxoisothiazolidinyl,    2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl,    thioxotriazolinyl, pyridinyl, piperidinyl, oxopiperidinyl,    2-oxo-1,3-diazacyclohexyl, morpholinyl or piperazinyl, which is    attached via N and is optionally substituted by nitro, cyano,    fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-,    s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl,    chlorodifluoromethyl, fluorodichloromethyl, methoxy, ethoxy, n- or    i-propoxy, n-, i-, s- or t-butoxy, difluoromethoxy,    trifluoromethoxy, chlorodifluoromethoxy, methylthio, ethylthio, n-    or i-propylthio, n-, i-, s- or t-butylthio, difluoromethylthio,    trifluoromethylthio, chlorodifluoromethylthio, methoxycarbonyl,    ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s- or    t-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl    or phenyl.-   R⁶ most preferably represents hydrogen, represents in each case    optionally fluorine-, chlorine-, methoxy- or ethoxy-substituted    methyl, ethyl, acetyl, methoxycarbonyl or ethoxycarbonyl.-   R⁶ especially preferably represents hydrogen, methyl or ethyl.

Preference according to the invention is given to the compounds of theformula (I) which contain a combination of the meanings listed above asbeing preferred.

Particular preference according to the invention is given to thecompounds of the formula (I) which contain a combination of the meaningslisted above as being particularly preferred.

Very particular preference according to the invention is given to thecompounds of the formula (I) which contain a combination of the meaningslisted above as being very particularly preferred.

A very particularly preferred group are those compounds of the formula(I) in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or methyl,-   R² represents cyano or trifluoromethyl,-   R³ represents hydrogen, chlorine or methyl,-   R⁴ represents hydrogen, fluorine or chlorine,-   R⁵ represents cyano, thiocarbamoyl, chlorine, bromine or    trifluoromethyl,-   R⁶ represents hydrogen, represents in each case optionally cyano-,    fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,    ethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl- or    ethoxycarbonyl-substituted methyl or ethyl, represents in each case    optionally cyano-, fluorine-, chlorine-, bromine-, methoxy- or    ethoxy-substituted acetyl, propionyl, methoxycarbonyl,    ethoxycarbonyl, represents in each case optionally fluorine- or    chlorine-substituted methylsulphonyl or ethylsulphonyl, represents    in each case optionally fluorine- or chlorine-substituted propenyl,    butenyl, propynyl or butynyl, represents in each case optionally    fluorine-, chlorine- or methyl-substituted cyclopropyl or    cyclopropylmethyl, cyclopropylcarbonyl or cyclopropylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,    benzoyl, phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl, and-   R⁷ represents methoxycarbonylmethoxy, ethoxycarbonylmethoxy, n- or    i-propoxycarbonylmethoxy, n-, i-, s- or t-butoxycarbonylmethoxy,    methoxycarbonylethoxy, ethoxycarbonylethoxy, n- or    i-propoxycarbonylethoxy, n-, i-, s- or t-butoxycarbonylethoxy,    methoxycarbonylmethylthio, ethoxycarbonylmethylthio, n- or    i-propoxycarbonylmethylthio, n-, i-, s- or    t-butoxycarbonylmethylthio, methoxycarbonylethylthio,    ethoxycarbonylethylthio, n- or i-propoxycarbonylethylthio, n-, i-,    s- or t-butoxycarbonylethylthio, propenyloxycarbonylmethoxy,    butenyloxycarbonylmethoxy, propenyloxycarbonylethoxy,    butenyloxycarbonylethoxy, propenyloxycarbonylmethylthio,    butenyloxycarbonylmethylthio, propenyloxycarbonylethylthio,    butenyloxycarbonylethylthio, propynyloxycarbonylmethoxy,    butynyloxycarbonylmethoxy, propynyloxycarbonylethoxy,    butynyloxycarbonylethoxy, propynyloxycarbonylmethylthio,    butynyloxycarbonylmethylthio, propynyloxycarbonylethylthio,    butynyloxycarbonylethylthio, methylaminocarbonylmethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylmethoxy, n-,    i-, s- or t-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,    ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-,    s- or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,    ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio,    n-, i-, s- or t-butylaminocarbonylmethylthio,    methylaminocarbonylethylthio, ethylaminocarbonylethylthio, n- or    i-propylaminocarbonylethylthio, n-, i-, s- or    t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,    diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,    diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,    diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,    diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,    dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,    dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,    dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio or    dipropynylaminocarbonylethylthio.

A further very particularly preferred group are those compounds of theformula (I) in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or methyl,-   R² represents cyano or trifluoromethyl,-   R³ represents hydrogen, chlorine or methyl,-   R⁴ represents hydrogen, fluorine or chlorine,-   R⁵ represents cyano, thiocarbamoyl, chlorine, bromine or    trifluoromethyl,-   R⁶ represents hydrogen, represents in each case optionally cyano-,    fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,    ethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl- or    ethoxycarbonyl-substituted methyl or ethyl, represents in each case    optionally cyano-, fluorine-, chlorine-, bromine-, methoxy- or    ethoxy-substituted acetyl, propionyl, methoxycarbonyl,    ethoxycarbonyl, represents in each case optionally fluorine- or    chlorine-substituted methylsulphonyl or ethylsulphonyl, represents    in each case optionally fluorine- or chlorine-substituted propenyl,    butenyl, propynyl or butynyl, represents in each case optionally    fluorine-, chlorine- or methyl-substituted cyclopropyl or    cyclopropylmethyl, cyclopropylcarbonyl or cyclopropylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,    benzoyl, phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl, and-   R⁷ represents hydroxyamino, represents N-methylhydroxyamino,    N-ethylhydroxyamino, N-n-propylhydroxyamino, N-i-propylhydroxyamino,    methoxyamino, ethoxyamino, n- or i-propoxyamino, n-, i-, s- or    t-butoxyamino, N-methylmethoxyamino, N-ethylmethoxyamino,    N-methylethoxyamino, methoxycarbonylmethoxyamino,    ethoxycarbonylmethoxyamino, n- or i-propoxycarbonylmethoxyamino,    methoxycarbonylethoxyamino, ethoxycarbonylethoxyamino, n- or    i-propoxycarbonylethoxyamino, N-methylmethoxycarbonylmethoxyamino,    N-methylethoxycarbonylmethoxyamino,    N-methyl-n-propoxycarbonylmethoxyamino,    N-methyl-i-propoxycarbonylmethoxyamino,    N-methyl-methoxycarbonylethoxyamino,    N-methylethoxycarbonylethoxyamino,    N-methyl-n-propoxycarbonylethoxyamino,    N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,    butenyloxyamino, N-methyl-propenyloxyamino, N-methylbutenyloxyamino,    N-propenylmethoxyamino, N-propenylethoxyamino,    N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino,    N-propenylpropenyloxyamino, or represents phenoxyamino or    N-methylphenoxyamino.

A further very particularly preferred group are those compounds of theformula (I) in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or methyl,-   R² represents cyano or trifluoromethyl,-   R³ represents hydrogen, chlorine or methyl,-   R⁴ represents hydrogen, fluorine or chlorine,-   R⁵ represents cyano, thiocarbamoyl, chlorine, bromine or    trifluoromethyl,-   R⁶ represents hydrogen, represents in each case optionally cyano-,    fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,    ethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl- or    ethoxycarbonyl-substituted methyl or ethyl, represents in each case    optionally cyano-, fluorine-, chlorine-, bromine-, methoxy- or    ethoxy-substituted acetyl, propionyl, methoxycarbonyl,    ethoxycarbonyl, represents in each case optionally fluorine- or    chlorine-substituted methylsulphonyl or ethylsulphonyl, represents    in each case optionally fluorine- or chlorine-substituted propenyl,    butenyl, propynyl or butynyl, represents in each case optionally    fluorine-, chlorine- or methyl-substituted cyclopropyl or    cyclopropylmethyl, cyclopropylcarbonyl or cyclopropylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,    benzoyl, phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diaza-cyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl, and-   R⁷ represents cyanoethylamino, cyanopropylamino or cyanobutylamino,    represents dimethylamino, diethylamino, di-n-propylamino,    di-i-propylamino, di-n-butylamino or di-i-butylamino, represents    N-methylcyanoethylamino, N-ethylcyanoethylamino,    N-n-propylcyanoethylamino, N-i-propylcyanoethylamino,    N-methylfluoroethylamino, N-ethylfluoroethylamino,    N-n-propylfluoroethylamino, N-i-propylfluoroethylamino,    N-methylmethoxyethylamino, N-ethylmethoxyethylamino,    N-methylethoxyethylamino, N-ethylethoxyethylamino,    N-methylmethoxycarbonylmethylamino,    N-methylethoxycarbonylmethylamino,    N-methylmethoxycarbonylethylamino, N-methylethoxycarbonylethylamino,    represents N-methyl-N-propenylamino, N-methyl-N-butenylamino,    N-ethyl-N-propenylamino, N-ethyl-N-butenylamino,    N-propyl-N-propenylamino, N-propyl-N-butenylamino,    N-butyl-N-propenylamino, N-butyl-N-butenylamino,    N-methyl-N-propynylamino, N-methyl-N-butynylamino,    N-ethyl-N-propynylamino, N-ethyl-N-butynylamino,    N-propyl-N-propynylamino, N-propyl-N-butynylamino,    N-butyl-N-propynylamino or N-butyl-N-butynylamino, or represents    dipropenylamino, dibutenylamino, dipropynylamino or dibutynylamino.

A further very particularly preferred group are those compounds of theformula (I) in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or methyl,-   R² represents cyano or trifluoromethyl,-   R³ represents hydrogen, chlorine or methyl,-   R⁴ represents hydrogen, fluorine or chlorine,-   R⁵ represents cyano, thiocarbamoyl, chlorine, bromine or    trifluoromethyl,-   R⁶ represents hydrogen, represents in each case optionally cyano-,    fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,    ethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl- or    ethoxycarbonyl-substituted methyl or ethyl, represents in each case    optionally cyano-, fluorine-, chlorine-, bromine-, methoxy- or    ethoxy-substituted acetyl, propionyl, methoxycarbonyl,    ethoxycarbonyl, represents in each case optionally fluorine- or    chlorine-substituted methylsulphonyl or ethylsulphonyl, represents    in each case optionally fluorine- or chlorine-substituted propenyl,    butenyl, propynyl or butynyl, represents in each case optionally    fluorine-, chlorine- or methyl-substituted cyclopropyl or    cyclopropylmethyl, cyclopropylcarbonyl or cyclopropylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,    benzoyl, phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl, and-   R⁷ represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, difluoromethyl-, dichloromethyl-, trifluoromethyl-,    chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n-    or i-propoxy-, n-, i-, s- or t-butoxy-, difluoromethoxy-,    trifluoromethoxy-, chlorodifluoromethoxy-, methylthio-, ethylthio-,    n- or i-propylthio-, n-, i-, s- or t-butylthio-,    difluoromethylthio-, trifluoromethylthio-,    chlorodifluoromethylthio-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-, n-, i-, s- or t-butoxycarbonyl-, cyclopropyl-,    cyclobutyl-, cyclopentyl-, cyclohexyl- or phenyl-substituted    heterocyclyloxy, heterocyclylthio, heterocyclylamino,    N-methylheterocyclylamino, N-methylheterocyclylmethylamino or    —N=(heterocyclyl), where the heterocyclyl grouping is selected from    the group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,    pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,    oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl,    thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl,    imidazolinyl, 2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl),    triazolyl, oxotriazolinyl, thioxotriazolinyl, pyridinyl,    piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl,    piperazinyl, pyrimidinyl.

A further very particularly preferred group are those compounds of theformula (I) in which

-   Q represents oxygen or sulphur,-   R¹ represents hydrogen, amino or methyl,-   R² represents cyano or trifluoromethyl,-   R³ represents hydrogen, chlorine or methyl,-   R⁴ represents hydrogen, fluorine or chlorine,-   R⁵ represents cyano, thiocarbamoyl, chlorine, bromine or    trifluoromethyl,-   R⁶ represents hydrogen, represents in each case optionally cyano-,    fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,    methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,    ethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl- or    ethoxycarbonyl-substituted methyl or ethyl, represents in each case    optionally cyano-, fluorine-, chlorine-, bromine-, methoxy- or    ethoxy-substituted acetyl, propionyl, methoxycarbonyl,    ethoxycarbonyl, represents in each case optionally fluorine- or    chlorine-substituted methylsulphonyl or ethylsulphonyl, represents    in each case optionally fluorine- or chlorine-substituted propenyl,    butenyl, propynyl or butynyl, represents in each case optionally    fluorine-, chlorine- or methyl-substituted cyclopropyl or    cyclopropylmethyl, cyclopropylcarbonyl or cyclopropylsulphonyl,    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,    difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,    fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- or    i-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,    benzoyl, phenylacetyl, phenylsulphonyl or phenylmethylsulphonyl, or    represents in each case optionally nitro-, cyano-, fluorine-,    chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or    t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,    fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-,    s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,    chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,    ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s- or    t-butoxycarbonyl-substituted heterocyclylcarbonyl,    heterocyclylmethylcarbonyl, heterocyclylsulphonyl or    heterocyclylmethylsulphonyl, where the heterocyclyl grouping is    selected from the group consisting of furyl, tetrahydrofuryl,    thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl,    pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl,    thiazolyl, thiazolinyl, thiazolidinyl, cyanoiminothiazolidinyl,    imidazolyl, imidazolinyl, 2-oxo-1,3-diazacyclopentyl    (2-oxoimidazolidinyl), triazolyl, oxotriazolinyl, thioxotriazolinyl,    pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,    morpholinyl, piperazinyl, and-   R⁷ represents a monocyclic or bicyclic nitrogen heterocycle from the    group consisting of pyrrolyl, pyrrolinyl, pyrrolidinyl,    oxopyrrolidinyl, pyrazolyl, imidazolyl, imidazolinyl,    2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl),    2-oxo-1,3-oxazacyclopentyl (2-oxooxazolidinyl), isoxazolidinyl,    thiazolinyl, 2-oxothiazolidinyl, 1,1-dioxoisothiazolidinyl,    2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl,    thioxotriazolinyl, pyridinyl, piperidinyl, oxopiperidinyl,    2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl, which is    attached via N and is optionally substituted by nitro, cyano,    fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-,    s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl,    chlorodifluoromethyl, fluorodichloromethyl, methoxy, ethoxy, n- or    i-propoxy, n-, i-, s- or t-butoxy, difluoromethoxy,    trifluoromethoxy, chlorodifluoromethoxy, methylthio, ethylthio, n-    or i-propylthio, n-, i-, s- or t-butylthio, difluoromethylthio,    trifluoromethylthio, chlorodifluoromethylthio, methoxycarbonyl,    ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s- or    t-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl    or phenyl.

The general or preferred radical definitions listed above apply both tothe end products of the formula (I) and, correspondingly, to thestarting materials or intermediates required in each case for thepreparation. These radical definitions can be combined with one anotheras desired, i.e. including combinations between the given preferredranges.

The novel substituted (thioxo)carbonylaminophenyluracils of the generalformula (I) have potent and selective herbicidal activity.

The novel substituted (thioxo)carbonylaminophenyluracils of the generalformula (I) are obtained with iso(thio)cyanatophenyluraciles of thegeneral formula (II)

in which

-   Q, R¹, R², R³, R⁴ and R⁵ are as defined above,    are reacted with compounds of the general formula (III)    H—R⁷  (III)    in which-   R⁷ is as defined above,    if appropriate in the presence of one or more reaction auxiliaries    and if appropriate in the presence of one or more diluents,    and the resulting substituted (thioxo)carbonylaminophenyluracils of    the general formula (Ia)

in which

-   Q, R¹, R², R³, R⁴, R⁵ and R⁷ are as defined above    are, if appropriate, reacted with compounds of the general formula    (IV)    X—R⁶  (IV)    in which-   R⁶ is as defined above, except for hydrogen, and-   X represents halogen (in particular chlorine, bromine or iodine), or    optionally also represents acetyloxy, propionyloxy,    methoxysulphonyloxy or ethoxysulphonyloxy,    if appropriate in the presence of one or more reaction auxiliaries    and if appropriate in the presence of one or more diluents.

Using, for example,3-(2,4-dichlorio-5-isothiocyanatophenyl)-1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dioneand N,O-dimethylhydroxylamine as starting materials, the course of thereaction in the process according to the invention can be illustrated bythe formula scheme below:

The formula (II) provides a general definition of the(thioxo)carbonylaminophenyluracils to be used as starting materials inthe process according to the invention for preparing compounds of theformula (I). In the formula (II), Q, R¹, R², R³, R⁴ and R⁵ preferablyhave those meanings which have already been mentioned above, inconnection with the description of the compounds of the formula (I)according to the invention, as being preferred, particularly preferredor very particularly preferred for Q, R¹, R², R³, R⁴ and R⁵.

Except for the compound3-(4-chloro-2-fluoro-5-isothiocyanatophenyl)-1-methyl-6-trifluoromethyl-2,4-(1H,3H)-pyrimidinedione(cf. U.S. Pat. No. 6,303,783), the starting materials of the generalformula (II) have hitherto not been disclosed in the literature; exceptfor the compound3-(4-chloro-2-fluoro-5-isothiocyanatophenyl)-1-methyl-6-trifluoromethyl-2,4-(1H,3H)-pyrimidinedionethey also form, as novel substances, part of the subject-matter of thepresent application.

The iso(thio)cyanatophenyluracils of the general formula (II) areobtained when aminophenyluracils of the general formula (V)

in which

-   R¹, R², R³, R⁴ and R⁵ are as defined above,    are reacted with phosgene (or diphosgene) or thiophosgene, if    appropriate in the presence of a reaction auxiliary such as, for    example, diazabicyclo[2.2.2]octane, and in the presence of a    diluent, such as, for example, acetone, toluene, xylene or    chlorobenzene, at temperatures between 0° C. and 150° C., and the    volatile components are distilled off under reduced pressure after    the reaction has ended (cf. the Preparation Examples). The compounds    of the formula (V) are known compounds.

The formulae (III) and (IV) provide general definitions of the compoundsfurther to be used as starting materials. Here, R⁶ and R⁷ preferablyhave those meanings which have already been mentioned above, inconnection with the description of the compounds of the formula (I)according to the invention, as being preferred, particularly preferred,very particularly preferred or most preferred for R⁶ and R⁷,respectively.

The starting materials of the formulae (III) and (IV) are knownchemicals of synthesis.

The process according to the invention for preparing the compounds ofthe general formula (I) is preferably carried out using a reactionauxiliary. Reaction auxiliaries suitable for the process according tothe invention are, in general, the customary inorganic or organic basesor acid acceptors. These preferably include alkali metal or alkalineearth metal acetates, amides, carbonates, bicarbonates, hydrides,hydroxides or alkoxides, such as, for example, sodium acetate, potassiumacetate or calcium acetate, lithium amide, sodium amide, potassium amideor calcium amide, sodium carbonate, potassium carbonate or calciumcarbonate, sodium bicarbonate, potassium bicarbonate or calciumbicarbonate, lithium hydride, sodium hydride, potassium hydride orcalcium hydride, lithium hydroxide, sodium hydroxide, potassiumhydroxide or calcium hydroxide, sodium methoxide, ethoxide, n- ori-propoxide, n-, i-, s- or t-butoxide or potassium methoxide, ethoxide,n- or i-propoxide, n-, i-, s- or t-butoxide; furthermore also basicorganic nitrogen compounds, such as, for example, trimethylamine,triethylamine, tripropylamine, tributylamine, ethyldiisopropylamine,N,N-dimethylcyclohexylamine, dicyclohexylamine, ethyldicyclohexylamine,N,N-dimethylaniline, N,N-dimethylbenzylamine, pyridine, 2-methyl-,3-methyl-, 4-methyl-, 2,4-dimethyl-, 2,6-dimethyl-, 3,4-dimethyl- and3,5-dimethylpyridine 5-ethyl-2-methylpyridine, 4-dimethylaminopyridine,N-methylpiperidine, 1,4-diazabicyclo[2.2.2]octane (DABCO),1,5-diazabicyclo[4.3.0]non-5-ene (DBN) or1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

The process according to the invention for preparing the compounds ofthe general formula (I) is preferably carried out using a diluent.Diluents suitable for carrying out the process according to theinvention are especially inert organic solvents. These include, inparticular, aliphatic, alicyclic or aromatic, optionally halogenatedhydrocarbons, such as benzine, benzene, toluene, xylene, chlorobenzene,dichlorobenzene, petroleum ether, hexane, cyclohexane, dichloromethane,chloroform, carbon tetrachloride; ethers, such as diethyl ether,diisopropyl ether, dioxane, tetrahydrofuran or ethylene glycol dimethylether or ethylene glycol diethyl ether; ketones, such as acetone,butanone or methyl isobutyl ketone; nitrites, such as acetonitrile,propionitrile or butyronitrile; amides, such as N,N-dimethylformamide,N,N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone orhexamethylphosphoric triamide; esters, such as methyl acetate or ethylacetate; sulphoxides, such as dimethyl sulphoxide; alcohols, such asmethanol, ethanol, n- or i-propanol, ethylene glycol monomethyl ether,ethylene glycol monoethyl ether, diethylene glycol monomethyl ether,diethylene glycol monoethyl ether, mixtures thereof with water or purewater.

When carrying out the process according to the invention, the reactiontemperatures can be varied within a relatively wide range. In general,the process is carried out at temperatures between 0° C. and 150° C.,preferably between 10° C. and 120° C.

The process according to the invention is generally carried out underatmospheric pressure. However, it is also possible to carry out theprocess according to the invention under elevated or reduced pressure—ingeneral between 0.1 bar and 10 bar.

For carrying out the process according to the invention, the startingmaterials are generally employed in approximately equimolar amounts.However, it is also possible to use a relatively large excess of one ofthe components. The reaction is generally carried out in a suitablediluent in the presence of a reaction auxiliary and the reaction mixtureis generally stirred at the required temperature for a number of hours.Work-up is carried out by customary methods (cf. the PreparationExamples).

The active compounds according to the invention can be used asdefoliants, desiccants, haulm killers and, especially, as weed killers.Weeds in the broadest sense are understood to mean all plants which growin locations where they are undesired. Whether the substances accordingto the invention act as total or selective herbicides dependsessentially on the amount used.

The active compounds according to the invention can be used, forexample, in connection with the following plants:

Dicotyledonous weeds of the genera: Abutilon, Amaranthus, Ambrosia,Anoda, Anthemis, Aphanes, Atriplex, Bellis, Bidens, Capsella, Carduus,Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium,Emex, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Hibiscus,Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha,Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum,Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola,Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea,Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola,Xanthium.

Dicotyledonous crops of the genera: Arachis, Beta, Brassica, Cucumis,Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca,Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia.

Monocotyledonous weeds of the genera: Aegilops, Agropyron, Agrostis,Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina,Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis,Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera,Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum,Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria,Sorghum.

Monocotyledonous crops of the genera: Allium, Ananas, Asparagus, Avena,Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale,Triticum, Zea.

However, the use of the active compounds according to the invention isin no way restricted to these genera, but also extends in the samemanner to other plants.

The active compounds according to the invention are suitable, dependingon the concentration, for the total control of weeds, for example onindustrial terrain and rail tracks, and on paths and areas with andwithout tree plantings. Similarly, the active compounds according to theinvention can be employed for controlling weeds in perennial crops, forexample forests, decorative tree plantings, orchards, vineyards, citrusgroves, nut orchards, banana plantations, coffee plantations, teaplantations, rubber plantations, oil palm plantations, cocoaplantations, soft fruit plantings and hop fields, on lawns, turf andpastureland, and for the selective control of weeds in annual crops.

The compounds of the formula (I) according to the invention have strongherbicidal activity and a broad active spectrum when used on the soiland on above-ground parts of plants. To a certain extent they are alsosuitable for the selective control of monocotyledonous anddicotyledonous weeds in monocotyledonous and dicotyledonous crops, bothby the pre-emergence and by the post-emergence method.

At certain concentrations or application rates, the active compoundsaccording to the invention can also be employed for controlling animalpests and fungal or bacterial plant diseases. If appropriate, they canalso be used as intermediates or precursors for the synthesis of otheractive compounds.

All plants and plant parts can be treated in accordance with theinvention. Plants are to be understood as meaning in the present contextall plants and plant populations such as desired and undesired wildplants or crop plants (including naturally occurring crop plants). Cropplants can be plants which can be obtained by conventional plantbreeding and optimization methods or by biotechnological and geneticengineering methods or by combinations of these methods, including thetransgenic plants and inclusive of the plant cultivars protectable ornot protectable by plant breeders' rights. Plant parts are to beunderstood as meaning all parts and organs of plants above and below theground, such as shoot, leaf, flower and root, examples which may bementioned being leaves, needles, stalks, stems, flowers, fruit bodies,fruits, seeds, roots, tubers and rhizomes. The plant parts also includeharvested material, and vegetative and generative propagation material,for example cuttings, tubers, rhizomes, offsets and seeds.

Treatment according to the invention of the plants and plant parts withthe active compounds is carried out directly or by allowing thecompounds to act on their surroundings, environment or storage space bythe customary treatment methods, for example by immersion, spraying,evaporation, fogging, scattering, painting on and, in the case ofpropagation material, in particular in the case of seeds, also byapplying one or more coats.

The active compounds can be converted into the customary formulationssuch as solutions, emulsions, wettable powders, suspensions, powders,dusts, pastes, soluble powders, granules, suspension-emulsionconcentrates, natural and synthetic materials impregnated with activecompound, and microencapsulations in polymeric materials.

These formulations are produced in a known manner, for example by mixingthe active compounds with extenders, that is, liquid solvents and/orsolid carriers, optionally with the use of surfactants, that is,emulsifiers and/or dispersants, and/or foam formers.

If the extender used is water, it is also possible, for example, to useorganic solvents as cosolvents. The following are essentially suitableas liquid solvents: aromatics such as xylene, toluene oralkylnaphthalenes, chlorinated aromatics and chlorinated aliphatichydrocarbons such as chlorobenzenes, chloroethylenes or methylenechloride, aliphatic hydrocarbons such as cyclohexane or paraffins, forexample mineral oil fractions, mineral and vegetable oils, alcohols suchas butanol or glycol and their ethers and esters, ketones such asacetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone,strongly polar solvents such as dimethylformamide and dimethylsulphoxide, or else water.

Suitable solid carriers are: for example ammonium salts and groundnatural minerals such as kaolins, clays, talc, chalk, quartz,attapulgite, montmorillonite or diatomaceous earth, and ground syntheticmaterials such as highly-disperse silica, alumina and silicates;suitable solid carriers for granules are: for example crushed andfractionated natural rocks such as calcite, marble, pumice, sepioliteand dolomite, or else synthetic granules of inorganic and organic meals,and granules of organic material such as sawdust, coconut shells, maizecobs and tobacco stalks; suitable emulsifiers and/or foam formers are:for example nonionic and anionic emulsifiers such as polyoxyethylenefatty acid esters, polyoxyethylene fatty alcohol ethers, for examplealkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates,arylsulphonates, or else protein hydrolysates; suitable dispersants are:for example lignin-sulphite waste liquors and methylcellulose.

Tackifiers such as carboxymethylcellulose and natural and syntheticpolymers in the form of powders, granules or latices, such as gumarabic, polyvinyl alcohol and polyvinyl acetate, or else naturalphospholipids such as cephalins and lecithins and syntheticphospholipids can be used in the formulations. Other additives can bemineral and vegetable oils.

It is possible to use colorants such as inorganic pigments, for exampleiron oxide, titanium oxide and Prussian Blue, and organic colorants suchas alizarin colorants, azo colorants and metal phthalocyanine colorants,and trace nutrients such as salts of iron, manganese, boron, copper,cobalt, molybdenum and zinc.

The formulations generally comprise between 0.1 and 95% by weight ofactive compound, preferably between 0.5 and 90%.

For controlling weeds, the active compounds according to the invention,as such or in their formulations, can also be used as mixtures withknown herbicides and/or substances which improve the compatibility withcrop plants (“safeners”), finished formulations or tank mixes beingpossible. Also possible are mixtures with weed-killers comprising one ormore known herbicides and a safener.

Possible components for the mixtures are known herbicides, for example

acetochlor, acifluorfen (-sodium), aclonifen, alachlor, alloxydim(-sodium), ametryne, amicarbazone, amidochlor, amidosulfuron, anilofos,asulam, atrazine, azafenidin, azimsulfuron, beflubutamid, benazolin(-ethyl), benfuresate, bensulfuron (-methyl), bentazone, benzfendizone,benzobicyclon, benzofenap, benzoylprop (-ethyl), bialaphos, bifenox,bispyribac (-sodium), bromobutide, bromofenoxim, bromoxynil, butachlor,butafenacil (-allyl), butroxydim, butylate, cafenstrole, caloxydim,carbetamide, carfentrazone (-ethyl), chlomethoxyfen, chloramben,chloridazone, chlorimuron (-ethyl), chlornitrofen, chlorsulfuron,chlortoluron, cinidon (-ethyl), cinmethylin, cinosulfuron, clefoxydim,clethodim, clodinafop (-propargyl), clomazone, clomeprop, clopyralid,clopyrasulfuron (-methyl), cloransulam (-methyl), cumyluron, cyanazine,cybutryne, cycloate, cyclosulfamuron, cycloxydim, cyhalofop (-butyl),2,4-D, 2,4-DB, desmedipham, diallate, dicamba, dichlorprop (-P),diclofop (-methyl), diclosulam, diethatyl (-ethyl), difenzoquat,diflufenican, diflufenzopyr, dimefuron, dimepiperate, dimethachlor,dimethametryn, dimethenamid, dimexyflam, dinitramine, diphenamid,diquat, dithiopyr, diuron, dymron, epropodan, EPTC, esprocarb,ethalfluralin, ethametsulfuron (-methyl), ethofumesate, ethoxyfen,ethoxysulfuron, etobenzanid, fenoxaprop (-P-ethyl), fentrazamide,flamprop (-isopropyl, -isopropyl-L, -methyl), flazasulfuron, florasulam,fluazifop (-P-butyl), fluazolate, flucarbazone (-sodium), flufenacet,flufenpyr, flumetsulam, flumiclorac (-pentyl), flumioxazin, flumipropyn,flumetsulam, fluometuron, fluorochloridone, fluoroglycofen (-ethyl),flupoxam, flupropacil, flurpyrsulfuron (-methyl, -sodium), flurenol(-butyl), fluridone, fluroxypyr (-butoxypropyl, -meptyl), flurprimidol,flurtamone, fluthiacet (-methyl), fluthiamide, fomesafen, foramsulfuron,glufosinate (-ammonium), glyphosate (-isopropylammonium), halosafen,haloxyfop (-ethoxyethyl, -P-methyl), hexazinone, imazamethabenz(-methyl), imazamethapyr, imazamox, imazapic, imazapyr, imazaquin,imazethapyr, imazosulfuron, iodosulfuron (-methyl, -sodium), ioxynil,isopropalin, isoproturon, isouron, isoxaben, isoxachlortole,isoxaflutole, isoxapyrifop, ketospiradox, lactofen, lenacil, linuron,MCPA, mecoprop, mefenacet, mesotrione, metamitron, metazachlor,methabenzthiazuron, metobenzuron, metobromuron, (alpha-) metolachlor,metosulam, metoxuron, metribuzin, metsulfuron (-methyl), molinate,monolinuron, naproanilide, napropamide, neburon, nicosulfuron,norflurazon, orbencarb, oryzalin, oxadiargyl, oxadiazon, oxasulfuron,oxaziclomefone, oxyfluorfen, paraquat, pelargonic acid, pendimethalin,pendralin, penoxysulam, pentoxazone, pethoxamide, phenmedipham,picolinafen, piperophos, pretilachlor, primisulfuron (-methyl),profluazol, profoxydim, prometryn, propachlor, propanil, propaquizafop,propisochlor, propoxycarbazone (-sodium), propyzamide, prosulfocarb,prosulfuron, pyraflufen (-ethyl), pyrazogyl, pyrazolate, pyrazosulfuron(-ethyl), pyrazoxyfen, pyribenzoxim, pyributicarb, pyridate, pyridatol,pyriftalid, pyriminobac (-methyl), pyrithiobac (-sodium), quinchlorac,quimnerac, quinoclamine, quizalofop (-P-ethyl, -P-tefuryl), rimsulfuron,sethoxydim, simazine, simetryn, sulcotrione, sulfentrazone, sulfometuron(-methyl), sulfosate, sulfosulfuron, tebutam, tebuthiuron, tepraloxydim,terbuthylazine, terbutryn, thenylchlor, thiafluamide, thiazopyr,thidiazimin, thifensulfuron (-methyl), thiobencarb, tiocarbazil,tralkoxydim, triallate, triasulfuron, tribenuron (-methyl), triclopyr,tridiphane, trifluralin, trifloxysulfuron, triflusulfuron (-methyl),tritosulfuron.

Also suitable for the mixtures are known safeners, for example AD-67,BAS-145138, benoxacor, cloquintocet (-mexyl), cymetrinil, 2,4-D, DKA-24,dichlormid, dymron, fenclorim, fenchlorazole (-ethyl), flurazole,fluxofenim, furilazole, isoxadifen (-ethyl), MCPA, mecoprop (-P),mefenpyr (-diethyl), MG-191, oxabetrinil, PPG-1292, R-29148.

A mixture with other known active compounds, such as fungicides,insecticides, acaricides, nematicides, bird repellents, plant nutrientsand agents which improve soil structure, is also possible.

The active compounds can be used as such, in the form of theirformulations or in the use forms prepared therefrom by further dilution,such as ready-to-use solutions, suspensions, emulsions, powders, pastesand granules. They are used in a customary manner, for example bywatering, spraying, atomizing or broadcasting.

The active compounds according to the invention can be applied bothbefore and after emergence of the plants. They can also be incorporatedinto the soil before sowing.

The amount of active compound used can vary within a relatively widerange. It depends essentially on the nature of the desired effect. Ingeneral, the amounts used are between 1 g and 10 kg of active compoundper hectare of soil surface, preferably between 5 g and 5 kg per ha.

As already mentioned above, it is possible to treat all plants and theirparts according to the invention. In a preferred embodiment, wild plantspecies and plant cultivars, or those obtained by conventionalbiological breeding methods, such as crossing or protoplast fusion, andparts thereof, are treated. In a further preferred embodiment,transgenic plants and plant cultivars obtained by genetic engineering,if appropriate in combination with conventional methods (GeneticallyModified Organisms), and parts thereof are treated. The term “parts” or“parts of plants” or “plant parts” has been explained above.

Particularly preferably, plants of the plant cultivars which are in eachcase commercially available or in use are treated according to theinvention. Plant cultivars are understood as meaning plants withparticular properties (“traits”) which are grown by conventionalcultivation, by mutagenesis or by recombinant DNA techniques. These maybe cultivars, biotypes or genotypes.

Depending on the plant species or plant cultivars, their location andgrowth conditions (soils, climate, vegetation period, diet), thetreatment according to the invention may also result in superadditive(“synergistic”) effects. Thus, for example, reduced application ratesand/or a widening of the activity spectrum and/or an increase in theactivity of the substances and compositions to be used according to theinvention—also in combination with other agrochemical compounds, betterplant growth, increased tolerance to high or low temperatures, increasedtolerance to drought or to water or soil salt content, increasedflowering performance, easier harvesting, accelerated maturation, higherharvest yields, better quality and/or a higher nutritional value of theharvested products, better storage stability and/or processability ofthe harvested products are possible which exceed the effects which wereactually to be expected.

The transgenic plants or plant cultivars (i.e. those obtained by geneticengineering) which are preferably to be treated according to theinvention include all plants which, in the genetic modification,received genetic material which imparts particularly advantageous usefulproperties (“traits”) to these plants. Examples of such properties arebetter plant growth, increased tolerance to high or low temperatures,increased tolerance to drought or to water or soil salt content,increased flowering performance, easier harvesting, acceleratedmaturation, higher harvest yields, better quality and/or a highernutritional value of the harvested products, better storage stabilityand/or processability of the harvested products. Further andparticularly emphasized examples of such properties are a better defenseof the plants against animal and microbial pests, such as againstinsects, mites, phytopathogenic fungi, bacteria and/or viruses, and alsoincreased tolerance of the plants to certain herbicidally activecompounds. Examples of transgenic plants which may be mentioned are theimportant crop plants, such as cereals (wheat, rice), maize, soya beans,potatoes, cotton, oilseed rape and also fruit plants (with the fruitsapples, pears, citrus fruits and grapes), and particular emphasis isgiven to maize, soya beans, potatoes, cotton and oilseed rape. Traitsthat are emphasized are in particular increased defence of the plantsagainst insects by toxins formed in the plants, in particular thoseformed in the plants by the genetic material from Bacillus thuringiensis(for example by the genes CryIA(a), CryIA(b), CryIA(c), CrylIA, CryIIIA,CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CryIF and also combinations thereof)(hereinbelow referred to as “Bt plants”). Traits which are alsoparticularly emphasized are the increased resistance of plants to fungi,bacteria and viruses by systemic acquired resistance (SAR), systemin,phytoalexins, elicitors and resistance genes and the correspondinglyexpressed proteins and toxins. Traits that are furthermore particularlyemphasized are the increased tolerance of the plants to certainherbicidally active compounds, for example imidazolinones,sulphonylureas, glyphosate or phosphinotricin (for example the “PAT”gene). The genes which impart the desired traits in question can also bepresent in combination with one another in the transgenic plants.Examples of “Bt plants” which may be mentioned are maize varieties,cotton varieties, soya bean varieties and potato varieties which aresold under the trade names YIELD GARD® (for example maize, cotton, soyabeans), KnockOut® (for example maize), StarLink® (for example maize),Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato). Examples ofherbicide-tolerant plants which may be mentioned are maize varieties,cotton varieties and soya bean varieties which are sold under the tradenames Roundup Ready® (tolerance to glyphosate, for example maize,cotton, soya bean), Liberty Link® (tolerance to phosphinothricin, forexample oilseed rape), IMI® (tolerance to imidazolinones) and STS®(tolerance to sulphonylureas, for example maize). Herbicide-resistantplants (plants bred in a conventional manner for herbicide tolerance)which may be mentioned include the varieties sold under the nameClearfield® (for example maize). Of course, these statements also applyto plant cultivars having these genetic traits or genetic traits stillto be developed, which cultivars will be developed and/or marketed inthe future.

The plants listed can be treated according to the invention in aparticularly advantageous manner with the compounds of the formula I orthe active compound mixtures according to the invention where, inaddition to the efficient control of the weed plants, the abovementionedsynergistic effects with the transgenic plants or plant cultivars mayoccur. The preferred ranges stated above for the active compounds ormixtures also apply to the treatment of these plants. Particularemphasis is given to the treatment of plants with the compounds ormixtures specifically mentioned in the present text.

The active compounds are also suitable for controlling animal pests, inparticular insects, arachnids and nematodes encountered in agriculture,in forests, in the protection of stored products and the protection ofmaterials and in the hygiene sector. They can preferably be used ascrop-protecting agents. They are effective against normally sensitiveand resistant species and against all or some stages of development.

When used as insecticides, the active compounds according to theinvention can furthermore be present in their commercial formulationsand in the use forms prepared from these formulations as a mixture withsynergists. Synergists are compounds which enhance the action of theactive compounds without it being necessary for the added synergist tobe active for its part.

The active compound content of the use forms prepared from thecommercial formulations can vary within wide ranges. The active compoundconcentration of the use forms can be from 0.0000001 to 95% by weight ofactive compound, and is preferably from 0.0001 to 1% by weight.

Application is carried out in a manner suitable for the use forms.

The active compounds of the formula (I) according to the invention arealso suitable for controlling arthropods which infest agriculturalproductive livestock, such as, for example, cattle, sheep, goats,horses, pigs, donkeys, camels, buffalo, rabbits, chickens, turkeys,ducks, geese and bees, other pets, such as, for example, dogs, cats,caged birds and aquarium fish, and also so-called test animals, such as,for example, hamsters, guinea pigs, rats and mice. By controlling thesearthropods, cases of death and reduction in productivity (for meat,milk, wool, hides, eggs, honey etc.) should be diminished, so that moreeconomic and easier animal husbandry is possible by use of the activecompounds according to the invention.

The active compounds according to the invention are used in theveterinary sector in a known manner by enteral administration in theform of, for example, tablets, capsules, potions, drenches, granules,pastes, boluses, the feed-through process and suppositories, byparenteral administration, such as, for example, by injection(intramuscular, subcutaneous, intravenous, intraperitoneal and thelike), implants, by nasal administration, by dermal use in the form, forexample, of dipping or bathing, spraying, pouring on and spotting on,washing and powdering, and also with the aid of moulded articlescontaining the active compound, such as collars, ear marks, tail marks,limb bands, halters, marking devices and the like.

When used for cattle, poultry, pets and the like, the active compoundsof the formula (I) can be used as formulations (for example powders,emulsions, free-flowing compositions), which comprise the activecompounds in an amount of 1 to 80% by weight, directly or after 100 to10 000-fold dilution, or they can be used as a chemical bath.

The active compounds are also suitable for controlling animal pests, inparticular insects, arachnids and mites, encountered in closed spaces,such as, for example, apartments, factory halls, offices, vehicle cabinsand the like. For controlling these pests, they can be used on their ownor in combination with other active compounds and auxiliaries inhousehold insecticide products. They are active against sensitive andresistant species and against all stages of development.

They are used in aerosols, pressure-free spray products, for examplepump and atomizer sprays, automatic fogging systems, foggers, foams,gels, evaporator products with evaporator tablets made of cellulose orpolymer, liquid evaporators, gel and membrane evaporators,propeller-driven evaporators, energy-free or passive evaporationsystems, moth papers, moth bags and moth gels, as granules or dusts, inbaits for spreading or in bait stations.

The preparation and the use of the active compounds according to theinvention is illustrated by the examples below.

PREPARATION EXAMPLES Example 1

A mixture of 2.50 g (6.1 mmol) of3-(4-bromo-2-fluoro-5-isocyanatophenyl)-1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione,0.96 g (6.1 mmol) of ethyl piperidine-3-carboxylate, 2 drops oftriethylamine and 30 ml of acetonitrile is stirred at room temperature(about 20° C.) for 15 hours and then concentrated under reducedpressure. The residue is worked up by column chromatography (silica gel,hexane/ethyl acetate, vol.: 2:1).

This gives 1.50 g (42% of theory) of ethyl1-[2-bromo-4-fluoro-5-(3-methyl-2,6-dioxo-4-trifluoromethyl-3,6-dihydro-2H-pyrimidin-1-yl)phenylcarbamoyl]piperidine-3-carboxylate.

logP (pH 2): 2.98

Analogously to Example 1 and in accordance with the general descriptionof the preparation process according to the invention, it is alsopossible to prepare, for example, the compounds of the general formula(I) listed in Table 1 below.

TABLE 1 (I)

Examples of compounds of the formula (I). In all cases, Q representsoxygen. Ex. Physical No. R¹ R² R³ R⁴ R⁵ R⁶ R⁷ data 2 CH₃ CF₃ H F Br H

logP = 2.51^(a)) 3 CH₃ CF₃ H F Br H

logP = 2.31^(a)) 4 CH₃ CF₃ H F Br H

logP = 2.73^(a)) 5 CH₃ CF₃ H F Br H

logP = 2.55^(a)) 6 CH₃ CF₃ H F Br H

logP = 2.85^(a)) 7 CH₃ CF₃ H F Br H

logP = 2.79^(a)) 8 CH₃ CF₃ H F Br H

logP = 2.67^(a)) 9 CH₃ CF₃ H F Br H

logP = 2.19^(a)) 10 CH₃ CF₃ H F Br H

logP = 3.06^(a)) 11 CH₃ CF₃ H F Cl H

logP = 3.50^(a)) 12 CH₃ CF₃ H F Cl H

logP = 3.11^(a)) 13 CH₃ CF₃ H F Cl H

logP = 2.80^(a)) 14 CH₃ CF₃ H F Cl H

logP = 2.55^(a)) 15 CH₃ CF₃ H F Cl H

logP = 2.06^(a)) 16 CH₃ CF₃ H F Br H

logP = 3.53^(a)) 17 CH₃ CF₃ H F Br H

logP = 3.15^(a)) 18 CH₃ CF₃ H F Br H

logP = 2.90^(a)) 19 CH₃ CF₃ H F Br H

logP = 2.59^(a)) 20 CH₃ CF₃ H F Br H

logP = 2.08^(a)) 21 CH₃ CF₃ H F Cl H

logP = 2.60^(a)) 22 CH₃ CF₃ H F Cl H

logP = 2.60^(a)) 23 CH₃ CF₃ H F Cl H

24 CH₃ CF₃ H F Cl H

logP = 2.58^(a)) 25 CH₃ CF₃ H F Cl H

logP = 2.55^(a)) 26 CH₃ CF₃ H F Br H

logP = 2.67^(a)) 27 CH₃ CF₃ H F Cl H

logP = 2.45^(a)) 28 CH₃ CF₃ H F Br H

logP = 2.63^(a)) 29 CH₃ CF₃ H F Br H

30 CH₃ CF₃ H F Br H

logP = 2.59^(a)) 31 CH₃ CF₃ H F Br H

logP = 2.59^(a)) 32 CH₃ CF₃ H F Cl H

logP = 2.51^(a)) 33 CH₃ CF₃ H F Br H

logP = 2.52^(a)) 34 CH₃ CF₃ H F Cl H

logP = 2.46^(a)) 35 CH₃ CF₃ H F Cl H

logP = 2.88^(a)) 36 CH₃ CF₃ H F Br H

logP = 2.88^(a)) 37 CH₃ CF₃ H F Br H

logP = 2.95^(a)) 38 CH₃ CF₃ H F Br H

logP = 2.79^(a)) 39 CH₃ CF₃ H F Br H

logP = 2.16^(a)) 40 CH₃ CF₃ H F Br H

logP = 2.06^(a)) 41 CH₃ CF₃ H F Br H

logP = 2.16^(a)) 42 CH₃ CF₃ H F Cl H

logP = 2.84^(a)) 43 CH₃ CF₃ H F Cl H

logP = 2.93^(a)) 44 CH₃ CF₃ H F Cl H

logP = 2.88^(a)) 45 CH₃ CF₃ H F Cl H

logP = 2.58^(a)) 46 CH₃ CF₃ H F Cl H

logP = 2.36^(a)) 47 CH₃ CF₃ H F Cl H

logP = 2.12^(a)) 48 CH₃ CF₃ H F Cl H

logP = 2.11^(a)) 49 CH₃ CF₃ H F Cl H

logP = 2.11^(a)) 50 CH₃ CF₃ H F CN H

M.p.: 130° C. 51 CH₃ CF₃ H F Cl H

logP = 2.52^(a)) 52 CH₃ CF₃ H F CN H

53 CH₃ CF₃ H F Cl H

logP = 2 2.81^(a)) 54 CH₃ CF₃ H F CN H

55 CH₃ CF₃ H F Cl H

56 CH₃ CF₃ H F Cl H

logP = 2.76^(a)) 57 CH₃ CF₃ H F CN H

58 CH₃ CF₃ H F CN H

¹H-NMR(DMSO-D₆, δ):6.58 ppm 59 CH₃ CF₃ H F CN H

¹H-NMR(DMSO-D₆, δ):6.58 ppm 60 CH₃ CF₃ H F CN H

¹H-NMR(DMSO-D₆, δ):6.58 ppm 61 CH₃ CF₃ H F CN H

¹H-NMR(DMSO-D₆, δ):6.55 ppm 62 CH₃ CF₃ H F Cl H

logP = 2.89^(a)) 63 CH₃ CF₃ H F Br H

logP = 2.96^(a)) 64 CH₃ CF₃ H F CN H

65 CH₃ CF₃ H F Cl H

logP = 2.78^(a)) 66 CH₃ CF₃ H F Br H

logP = 2.85^(a)) 67 CH₃ CF₃ H F CN H

68 CH₃ CF₃ H F Cl H

logP = 2.99^(a)) 69 CH₃ CF₃ H F Br H

logP = 3.06^(a)) 70 CH₃ CF₃ H F CN H

71 CH₃ CF₃ H F Cl H

logP = 3.35^(a)) 72 CH₃ CF₃ H F Br H

logP = 3.41^(a)) 73 CH₃ CF₃ H F CN H

74 CH₃ CF₃ H F Cl H

logP = 2.93^(a)) 75 CH₃ CF₃ H F Br H

logP = 3.01^(a)) 76 CH₃ CF₃ H F CN H

77 CH₃ CF₃ H F Cl CH₃

logP = 2.53^(a)) 78 CH₃ CF₃ H F Br CH₃

79 CH₃ CF₃ H F CN CH₃

80 CH₃ CF₃ H F Cl H

81 CH₃ CF₃ H F Br H

82 CH₃ CF₃ H F Cl H

83 CH₃ CF₃ H F Br H

84 CH₃ CF₃ H F Cl H

logP = 2.29^(a)) 85 CH₃ CF₃ H F Br H

logP = 2.35^(a)) 86 CH₃ CF₃ H F Cl H

logP = 2.29^(a)) 87 CH₃ CF₃ H F Br H

logP = 2.35^(a)) 88 CH₃ CF₃ H F Cl H

89 CH₃ CF₃ H F Br H

90 CH₃ CF₃ H F Cl H

91 CH₃ CF₃ H F Br H

92 CH₃ CF₃ H F Cl H

logP = 1.93^(a)) 93 CH₃ CF₃ H F Br H

logP = 1.97^(a)) 94 CH₃ CF₃ H F Cl H

logP = 1.74^(a)) 95 CH₃ CF₃ H F Br H

logP = 1.80^(a)) 96 CH₃ CF₃ H F Cl H

logP = 2.43^(a)) 97 CH₃ CF₃ H F Br H

logP = 2.47^(a)) 98 CH₃ CF₃ H F Cl H

logP = 3.02^(a)) 99 CH₃ CF₃ H F Br H

logP = 3.10^(a)) 100 CH₃ CF₃ H F Cl H

logP = 3.11^(a)) 101 CH₃ CF₃ H F Br H

logP = 3.16^(a)) 102 CH₃ CF₃ H F Cl H

logP = 2.38^(a)) 103 CH₃ CF₃ H F Br H

logP = 2.41^(a)) 104 CH₃ CF₃ H F Cl H

logP = 2.58^(a)) 105 CH₃ CF₃ H F Br H

logP = 2.62^(a)) 106 CH₃ CF₃ H F Cl

logP = 2.96^(a)) 107 CH₃ CF₃ H F Cl

logP = 2.72^(a)) 108 CH₃ CF₃ H F Cl

logP = 2.75^(a)) 109 CH₃ CF₃ H F Cl

logP = 2.56^(a)) 110 CH₃ CF₃ H F Cl

logP = 2.77^(a)) 111 CH₃ CF₃ H F Cl C₂H₅

logP = 2.80^(a)) 112 CH₃ CF₃ H F Br H

logP = 2.69^(a)) 113 CH₃ CF₃ H F Cl H

logP = 1.72^(a)) 114 CH₃ CF₃ H F Br H

115 CH₃ CF₃ H F Cl H

logP = 1.89^(a)) 116 CH₃ CF₃ H F Br H

logP = 1.93^(a)) 117 CH₃ CF₃ H F Cl H

logP = 1.77^(a)) 118 CH₃ CF₃ H F Br H

logP = 1.81^(a)) 119 CH₃ CF₃ H F Cl H

logP = 2.50^(a)) 120 CH₃ CF₃ H F Br H

logP = 2.55^(a)) 121 CH₃ CF₃ H F Cl H

logP = 2.48^(a)) 122 CH₃ CF₃ H F Br H

logP = 2.54^(a)) 123 CH₃ CF₃ H F Br H

logP = 3.07^(a)) 124 CH₃ CF₃ H F Cl H

logP = 2.56^(a)) 125 CH₃ CF₃ H F Br H

logP = 2.79^(a)) 126 CH₃ CF₃ H F Cl H

logP = 2.74^(a)) 127 CH₃ CF₃ H F Cl H

logP = 2.74^(a)) 128 CH₃ CF₃ H F CN H

logP = 2.80^(a)) 129 CH₃ CF₃ H F CN H

logP = 2.50^(a)) 130 CH₃ CF₃ H F CN H NH(CH₂)₅CN logP = 2.40^(a)) 131CH₃ CF₃ H F CN H

logP = 2.80^(a)) 132 CH₃ CF₃ H F CN H

logP = 2.88^(a)) 133 CH₃ CF₃ H F CN H

logP = 2.70^(a)) 134 CH₃ CF₃ H F CN H

logP = 2.02^(a)) 135 CH₃ CF₃ H F CN H N(CH₂CH═CH₂)₂ 136 CH₃ CF₃ H F CN H

The logP values given in the table were determined in accordance withEEC Directive 79/831 Annex V.A8 by HPLC (High Performance LiquidChromatography) using a reversed-phase column (C 18). Temperature: 43°C. ^(a))Mobile phases for the determination in the acidic range: 0.1%aqueous phosphoric acid, acetonitrile; linear gradient from 10%acetonitrile to 90% acetonitrile - the corresponding measurement resultsare marked ^(a)) in Table 1. ^(b))Mobile phases for the determination inthe neutral range: 0.01% molar aqueous phosphate buffer solution,acetonitrile; linear gradient from 10% acetonitrile to 90%acetonitrile - corresponding measurement results are marked ^(b)) inTable 1.

Calibration was carried out using unbranched alkan-2-ones (with 3 to 16carbon atoms) with known logP values (determination of the logP valuesby the retention times using linear interpolation between two successivealkanones).

The lambda max values were determined in the maxima of thechromatographic signals using the UV spectra from 200 nm to 400 nm.

Starting Materials of the Formula (II):

Example II-1

At about −20° C., 374.5 g (3.78 mol) of phosgene are initially chargedin 1000 ml of chlorobenzene and, after removal of the cooling bath, asolution of 241 g (0.63 mol) of3-(5-amino-4-bromo-2-fluorophenyl)-1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dionein 1000 ml of chlorobenzene is added dropwise with stirring, over aperiod of 20 minutes, during which the internal temperature increases toabout 10° C. The reaction mixture is then stirred at room temperature(about 20° C.) for about 30 minutes, then, with introduction of phosgene(about 280 g), heated to 120° C. and finally stirred at this temperaturefor about 60 minutes. For work-up, the volatile components are carefullydistilled off under reduced pressure (about 14 mbar).

This gives 276 g (86% of theory, purity of the product 80.6%) of3-(4-bromo-2-fluoro-5-isocyanatophenyl)-1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dionewhich can be used without further purification for preparing compoundsof the formula (I) according to the invention.

Example II-2

0.50 g (1.07 mmol) of3-(5-amino-4-cyano-2-fluorophenyl)-1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dioneis initially charged in 50 ml of acetone, 0.24 g (1.23 mmol) oftrichloromethyl chloroformate (“diphosgene”) is added dropwise and themixture is stirred at room temperature (about 20° C.) for 2 hours. Thevolatile components are then carefully distilled off under reducedpressure.

The product obtained in this manner as residue can be used withoutfurther purification for preparing compounds of the formula (I)according to the invention.

Analogously to Examples II-1 and II-2, it is also possible to prepare,for example, the compounds of the formula II listed in Table 2 below.

TABLE 2 (II)

Examples of compounds of the formula (II) Ex. Physical No. Q R¹ R² R³ R⁴R⁵ data II-3 O CH₃ CF₃ H F Cl II-4 O CH₃ CF₃ H Cl Cl II-5 O CH₃ CF₃ H ClBr II-6 O CH₃ CF₃ H H Cl II-7 O CH₃ CF₃ H H Br II-8 O CH₃ CF₃ H H CNUse Examples:

Example A

Pre-emergence test Solvent: 5 parts by weight of acetone Emulsifier: 1part by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent, thestated amount of emulsifier is added and the concentrate is diluted withwater to the desired concentration.

Seeds of the test plants are sown in normal soil. After 24 hours, thesoil is sprayed with the preparation of active compound such that theparticular amount of active compound desired is applied per unit area.The concentration of active compound in the spray liquor is chosen suchthat the particular amount of active compound desired is applied in 1000liters of water per hectare.

After three weeks, the degree of damage to the plants is rated in %damage in comparison to the development of the untreated control. Thefigures denote:

-   -   0%=no effect (like untreated control)    -   100%=total destruction

In this test, for example, the compounds of Preparation Examples 2, 3,4, 5, 6, 7, 8, 9, 10, 20, 21, 22, 24, 25, 26, 27, 28, 30, 31, 32, 37,38, 39, 44, 45, 46, 47, 48 and 49 exhibit strong activity against weeds,and some are tolerated well by crop plants, such as, for example, maize,wheat, soya bean and sugar beet.

Example B

Post-emergence test Solvent: 5 parts by weight of acetone Emulsifier: 1part by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent, thestated amount of emulsifier is added and the concentrate is diluted withwater to the desired concentration.

Test plants of a height of 5-15 cm are sprayed with the preparation ofactive compound such that the particular amounts of active compounddesired are applied per unit area. The concentration of the spray liquoris chosen such that the particular amounts of active compound desiredare applied in 1000 l of water/ha.

After three weeks, the degree of damage to the plants is rated in %damage in comparison to the development of the untreated control.

The figures denote:

-   -   0%=no effect (like untreated control)    -   100%=total destruction

In this test, for example, the compounds of Preparation Examples 2, 3,4, 5, 6, 7, 8, 9, 10, 21, 24, 25, 26, 27, 28, 30, 31, 32, 33, 34, 35,36, 37, 38, 39, 40, 41, 42, 44, 45, 46, 47 and 48 exhibit strongactivity against weeds, and some are tolerated well by crop plants, suchas, for example, wheat.

1. A compound of formula (I)

in which Q represents oxygen, R¹ represents hydrogen or amino; orrepresents optionally cyano-, halogen-, or C₁-C₄-alkoxy-substitutedalkyl having 1 to 6 carbon atoms, R² represents carboxyl, cyano,carbamoyl, or thiocarbamoyl; or represents optionally cyano-, halogen-,or C₁-C₄-alkoxy-substituted alkyl or alkoxy-carbonyl having in each case1 to 6 carbon atoms in the alkyl groups, R³ represents hydrogen orhalogen; or represents optionally halogen-substituted alkyl having 1 to6 carbon atoms, R⁴ represents hydrogen, cyano, carbamoyl, thiocarbamoyl,or halogen, R⁵ represents cyano, carbamoyl, thiocarbamoyl, or halogen;or represents optionally halogen-substituted alkyl or alkoxy having ineach case 1 to 6 carbon atoms, R⁶ represents hydrogen; representsoptionally cyano-, carboxyl-, halogen-, C₁-C₄-alkoxy-, C₁-C₄-alkylthio-,C₁-C₄-alkylsulphinyl-, C₁-C₄-alkylsulphonyl-, C₁-C₄-alkyl-carbonyl-, orC₁-C₄-alkoxy-carbonyl-substituted alkyl having 1 to 6 carbon atoms;represents optionally cyano-, halogen-, or C₁-C₄-alkoxy-substitutedalkylcarbonyl, alkoxycarbonyl, or alkylsulphonyl having in each case 1to 6 carbon atoms in the alkyl groups; represents optionallyhalogen-substituted alkenyl, alkenylcarbonyl, alkenylsulphonyl, oralkynyl having in each case 3 to 6 carbon atoms in the alkenyl oralkynyl groups; represents optionally cyano-, halogen-, orC₁-C₄-alkyl-substituted cycloalkyl, cycloalkylalkyl, cycloalkylcarbonyl,cycloalkylalkylcarbonyl, cycloalkylsulphonyl, orcycloalkylalkylsulphonyl having in each case 3 to 6 carbon atoms in thecycloalkyl groups and optionally 1 to 4 carbon atoms in the alkylmoiety; represents optionally nitro-, cyano-, halogen-, C₁-C₄-alkyl-,C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-, C₁-C₄-haloalkoxy-, orC₁-C₄-alkoxy-carbonyl-substituted aryl, arylalkyl, arylcarbonyl,arylalkylcarbonyl, arylsulfonyl, or arylalkylsulphonyl having in eachcase 6 or 10 carbon atoms in the aryl groups and optionally 1 to 4carbon atoms in the alkyl moiety; or represents optionally nitro-,cyano-, halogen-, C₁-C₄-alkyl-, C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-,C₁-C₄-haloalkoxy-, or C₁-C₄-alkoxy-carbonyl-substitutedheterocyclylcarbonyl, heterocyclylalkylcarbonyl, heterocyclylsulphonyl,or heterocyclylalkylsulphonyl having in each case up to 6 carbon atoms,up to 5 nitrogen atoms, and/or 1 or 2 oxygen or sulphur atoms as ringmembers, wherein each heterocyclyl group also optionally contains 1 or 2—SO groups, 1 or 2 —SO₂ groups, 1 or 2 —CO groups, or 1 or 2 —CS groups,and R⁷ represents optionally halogen-substituted alkoxycarbonylalkoxy,alkoxycarbonylalkylthio, alkenyloxycarbonylalkoxy,alkenyloxycarbonylalkylthio, alkynyloxycarbonylalkoxy,alkynyloxycarbonylalkylthio, carbamoylalkoxy, carbamoylalkylthio,alkylaminocarbonylalkoxy, alkylaminocarbonylalkylthio,dialkylaminocarbonylalkoxy, dialkylaminocarbonylalkylthio,N-alkyl-N-alkenylaminocarbonylalkoxy,N-alkyl-N-alkenylaminocarbonylalkylthio, dialkenylaminocarbonylalkoxy,dialkenylaminocarbonylalkylthio, N-alkyl-N-alkynylaminocarbonylalkoxy,N-alkyl-N-alkynylaminocarbonylalkylthio having in each case up to 6carbon atoms in the alkyl, alkenyl, or alkynyl groups; representshydroxyamino; represents optionally halogen-substitutedN-alkylhydroxyamino, alkoxyamino, N-alkylalkoxyamino,alkoxycarbonylalkoxyamino, or N-alkylalkoxycarbonylalkoxyamino having ineach case 1 to 6 carbon atoms in the alkyl groups; represents optionallyhalogen-substituted alkenyloxyamino, N-alkylalkenyloxyamino,N-alkenylalkoxyamino, or N-alkenylalkenyloxyamino having in each case 3to 6 carbon atoms in the alkenyl groups and optionally 1 to 6 carbonatoms in the alkyl groups; represents cycloalkyloxyamino orN-alkylcycloalkyloxyamino having in each case 3 to 6 carbon atoms in thecycloalkyl groups and optionally 1 to 6 carbon atoms in the alkyl group;represents optionally halogen-substituted aryloxyamino orN-alkylaryloxyamino having in each case 6 or 10 carbon atoms in the arylgroups and optionally 1 to 6 carbon atoms in the alkyl group; representscyanoalkylamino having 1 to 6 carbon atoms; represents optionallycyano-, halogen-, C₁-C₄-alkoxy-, or C₁-C₄-alkoxycarbonyl-substituteddialkylamino having in each case 1 to 6 carbon atoms in the alkylgroups; represents optionally cyano-, halogen-, orC₁-C₄-alkoxy-carbonyl-substituted N-alkyl-N-alkenylamino orN-alkyl-N-alkynylamino having in each case up to 6 carbon atoms in thealkyl, alkenyl, or alkynyl groups; represents dialkenylamino ordialkynylamino having in each case up to 6 carbon atoms in the alkenylor alkynyl groups; optionally nitro-, cyano-, halogen-, C₁-C₄-alkyl-,C₁-C₄-haloalkyl-, C₁-C₄-alkoxy-, C₁-C₄-haloalkoxy-, C₁-C₄-alkylthio-,C₁-C₄-haloalkylthio-, C₁-C₄-alkoxy-carbonyl-, C₃-C₆-cycloalkyl-, ormonocyclic or bicyclic phenyl-substituted heterocyclyloxy,heterocyclylthio, heterocyclylamino, N-alkylheterocyclylamino,N-alkylheterocyclylalkylamino, or —N=(heterocyclyl), where theheterocyclyl group contains up to 6 carbon atoms, up to 5 nitrogen atomsand/or 1 or 2 oxygen atoms and/or 1 or 2 sulphur atoms and optionallyadditionally 1 or 2 —SO groups and/or 1 or 2 —SO₂ groups and/or 1 or 2—CO groups and/or 1 or 2 —CS groups, and the alkyl group optionallycontains 1 to 6 carbon atoms; a monocyclic or bicyclic nitrogenheterocycle that is attached via N, contains up to 9 carbon atoms, up to5 nitrogen atoms, and optionally additionally 1 or 2 oxygen or sulphuratoms and optionally additionally 1 or 2 —SO groups, 1 or 2 —SO₂ groups,1 or 2 —CO groups, 1 or 2 —CS groups, or one cyanoimino group (C═N—CN)and is optionally substituted by nitro, cyano, halogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio,C₁-C₄-haloalkylthio, C₁-C₄-alkoxy-carbonyl,C₁-C₄-alkoxy-carbonyl-C₁-C₂-alkoxy, C₁-C₄-alkyl-carbonylamino,C₁-C₄-alkoxy-carbonylamino, C₂-C₄-alkylenedioxy, C₃-C₆-cycloalkyl, orphenyl.
 2. A compound of formula (I) according to claim 1 in which Qrepresents oxygen, R¹ represents hydrogen or amino; or representsoptionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, orn- or i-propoxy-substituted alkyl having 1 to 5 carbon atoms, R²represents carboxyl, cyano, carbamoyl, or thiocarbamoyl; or representsoptionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, orn- or i-propoxy-substituted alkyl or alkoxycarbonyl having in each case1 to 5 carbon atoms in the alkyl groups, R³ represents hydrogen,fluorine, chlorine, or bromine; or represents optionally fluorine-,chlorine-, or bromine-substituted alkyl having 1 to 5 carbon atoms, R⁴represents hydrogen, cyano, carbamoyl, thiocarbamoyl, fluorine,chlorine, or bromine, R⁵ represents cyano, carbamoyl, thiocarbamoyl,fluorine, chlorine, or bromine; or represents optionally fluorine-,chlorine-, or bromine-substituted alkyl or alkoxy having in each case 1to 5 carbon atoms, R⁶ represents hydrogen; represents optionally cyano-,carboxyl-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- ori-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-,methylsulphinyl-, ethylsulphinyl-, n- or i-propylsulphinyl-,methylsulphonyl-, ethylsulphonyl-, acetyl-, propionyl-, n- ori-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, or n- or-propoxycarbonyl-substituted alkyl having 1 to 5 carbon atoms;represents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,ethoxy-, or n- or i-propoxy-substituted alkylcarbonyl, alkoxycarbonyl,or alkylsulphonyl having in each case 1 to 5 carbon atoms in the alkylgroups; represents optionally fluorine-, chlorine-, orbromine-substituted alkenyl, alkenylcarbonyl, alkenylsulphonyl, oralkynyl having in each case 3 to 5 carbon atoms in the alkenyl oralkynyl groups; represents optionally cyano-, fluorine-, chlorine-,bromine-, methyl-, ethyl-, or n- or i-propyl-substituted cycloalkyl,cycloalkylalkyl, cycloalkylcarbonyl, cycloalkylalkylcarbonyl,cycloalkylsulphonyl, or cycloalkylalkylsulphonyl having in each case 3to 6 carbon atoms in the cycloalkyl groups and optionally 1 to 3 carbonatoms in the alkyl moiety; represents optionally nitro-, cyano-,fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-,i-, s-, or t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-,or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,ethoxycarbonyl-, n- or 1-propoxycarbonyl-, or n-, i-, s-, ort-butoxycarbonyl-substituted aryl, arylalkyl, arylcarbonyl,arylalkylcarbonyl, arylsulphonyl, or arylalkylsulphonyl having in eachcase 6 or 10 carbon atoms in the aryl groups and optionally 1 to 3carbon atoms in the alkyl moiety; or represents optionally nitro-,cyano-, fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- ori-propyl-, n-, i-, s-, or t-butyl-, trifluoromethyl-,chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n- ori-propoxy-, n-, i-, s-, or t-butoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, n- or -propoxycarbonyl-, or n-, i-,s-, or t-butoxycarbonyl-substituted heterocyclylcarbonyl,heterocyclylalkylcarbonyl, heterocyclylsulphonyl, orheterocyclylalkylsulphonyl having in each case up to 5 carbon atoms, upto 4 nitrogen atoms, and/or one oxygen or sulphur atom as ring members,wherein each heterocyclyl group also optionally contains an —SO group,an —SO₂ group, 1 or 2 —CO groups, or 1 or 2 —CS groups, and R⁷represents optionally halogen-substituted alkoxycarbonylalkoxy,alkoxycarbonylalkylthio, alkenyloxycarbonylalkoxy,alkenyloxycarbonylalkylthio, alkynyloxycarbonylalkoxy,alkynyloxycarbonylalkylthio, carbamoylalkoxy, carbamoylalkylthio,alkylaminocarbonylalkoxy, alkylaminocarbonylalkylthio,dialkylaminocarbonylalkoxy, dialkylaminocarbonylalkylthio,dialkenylaminocarbonylalkoxy, dialkenylaminocarbonylalkylthio,dialkynylaminocarbonyloxy, or dialkynylaminocarbonylalkylthio having ineach case up to 5 carbon atoms in the alkyl, alkenyl, or alkynyl groups;hydroxyamino; represents optionally halogen-substitutedN-alkylhydroxyamino, alkoxyamino, N-alkylalkoxyamino,alkoxycarbonylalkoxyamino, or N-alkylalkoxycarbonylalkoxyamino having ineach case 1 to 5 carbon atoms in the alkyl groups; represents optionallyhalogen-substituted alkenyloxyamino, N-alkyl-alkenyloxyamino,N-alkenylalkoxyamino or N-alkenylalkenyloxyamino having in each case 3to 5 carbon atoms in the alkenyl groups and optionally 1 to 5 carbonatoms in the alkyl groups; represents cycloalkyloxyamino orN-alkylcycloalkyloxyamino having in each case 3 to 6 carbon atoms in thecycloalkyl groups and optionally 1 to 3 carbon atoms in the alkyl group;represents optionally halogen-substituted aryloxyamino orN-alkylaryloxyamino having in each case 6 or 10 carbon atoms in the arylgroups and optionally 1 to 3 carbon atoms in the alkyl group; representscyanoalkylamino having 1 to 5 carbon atoms; represents optionallycyano-, fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted dialkylamino having in each case 1 to 5carbon atoms in the alkyl groups; represents optionally cyano-,fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted N-alkyl-N-alkenylamino orN-alkyl-N-alkynylamino having in each case up to 5 carbon atoms in thealkyl, alkenyl, or alkynyl groups; represents dialkenylamino ordialkynylamino having in each case up to 5 carbon atoms in the alkenylor alkynyl groups; represents optionally nitro-, cyano-, fluorine-,chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, ort-butyl-, difluoromethyl-, dichloromethyl-, trifluoromethyl-,chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n- or1-propoxy-, n-, i-, s-, or t-butoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, methylthio-, ethylthio-, n-or i-propylthio-, n-, i-, s- or t-butylthio-, difluoromethylthio-,trifluoromethylthio-, chlorodifluoromethylthio-, methoxycarbonyl-,ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s-, ort-butoxycarbonyl-, cyclopropyl-, cyclobutyl-, cyclopentyl-, cyclohexyl-,or phenyl-substituted heterocyclyloxy, heterocyclylthio,heterocyclylamino, N-alkylheterocyclylamino,N-alkylheterocyclylalkylamino, or —N=(heterocyclyl), where themonocyclic or bicyclic heterocyclyl group contains up to 6 carbon atoms,up to 5 nitrogen atoms, and/or 1 or 2 oxygen atoms and/or 1 or 2 sulphuratoms and optionally additionally 1 or 2 —SO groups and/or 1 or 2 —SO₂groups and/or 1 or 2 —CO groups and/or 1 or 2 —CS groups and the alkylgroup optionally contains 1 to 3 carbon atoms; represents a monocyclicor bicyclic nitrogen heterocycle that is attached via N, contains up to9 carbon atoms, up to 5 nitrogen atoms, and optionally additionally 1 or2 oxygen or sulphur atoms and optionally additionally 1 or 2 —SO groups,1 or 2 —SO₂ groups, 1 or 2 —CO groups, 1 or 2 —CS groups or onecyanoimino group (C═N—CN) and is optionally substituted by nitro, cyano,fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, 1-, s-,or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl,chlorodifluoromethyl, fluorodichloromethyl, methoxy, ethoxy, n- ori-propoxy, n-, i-, s-, or t-butoxy, difluoromethoxy, trifluoromethoxy,chlorodifluoromethoxy, methylthio, ethylthio, n- or i-propylthio, n-,i-, s-, or t-butylthio, difluoromethylthio, trifluoromethylthio,chlorodifluoromethylthio, methoxycarbonyl, ethoxycarbonyl, n- ori-propoxycarbonyl, n-, i-, s-, or t-butoxycarbonyl,methoxycarbonylmethoxy, ethoxycarbonylmethoxy, acetylamino,propionylamino, methoxycarbonylamino, ethoxycarbonylamino,ethylenedioxy, propylenedioxy, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, or phenyl.
 3. A compound of formula (I) according to claim 1in which R¹ represents hydrogen or amino; or represents optionallycyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, or n- ori-propoxy-substituted methyl, ethyl, n- or i-propyl, or n-, i-, ors-butyl, R² represents carboxyl, cyano, carbamoyl, or thiocarbamoyl; orrepresents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,ethoxy-, or n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl,methoxycarbonyl, ethoxycarbonyl, or n- or i-propoxycarbonyl, R³represents hydrogen, fluorine, chlorine, or bromine; or representsoptionally fluorine-, chlorine-, or bromine-substituted methyl, ethyl,or n- or i-propyl, R⁴ represents hydrogen, cyano, carbamoyl,thiocarbamoyl, fluorine, chlorine, or bromine, R⁵ represents cyano,carbamoyl, thiocarbamoyl, fluorine, chlorine, or bromine; or representsoptionally fluorine-, chlorine-, or bromine-substituted methyl, ethyl,n- or i-propyl, methoxy, ethoxy, or n- or -propoxy, R⁶ representshydrogen; represents optionally cyano-, carboxyl-, fluorine-, chlorine-,bromine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-,n- or i-propylthio-, methylsulphinyl-, ethylsulphinyl-, n- ori-propylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, acetyl-,propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, or n-or i-propoxycarbonyl-substituted methyl, ethyl, n- or i-propyl, or n-,i-, or s-butyl; represents optionally cyano-, fluorine-, chlorine-,bromine-, methoxy-, ethoxy-, or n- or i-propoxy-substituted acetyl,propionyl, n- or i-butyroyl, methoxycarbonyl, ethoxycarbonyl, n- ori-propoxycarbonyl, n-, i-, s-, or t-butoxycarbonyl, methylsulphonyl,ethylsulphonyl, n- or i-propylsulphonyl, or n-, i-, or s-butylsulphonyl;represents optionally fluorine-, chlorine-, or bromine-substitutedpropenyl, butenyl, propenylsulphonyl, butenylsulphonyl, propynyl, orbutynyl; represents optionally cyano-, fluorine-, chlorine-, bromine-,methyl-, or ethyl-substituted cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl,cyclohexylmethyl, cyclopropylcarbonyl, cyclobutylcarbonyl,cyclopentylcarbonyl, cyclohexylcarbonyl, cyclopropylmethylcarbonyl,cyclobutylmethylcarbonyl, cyclopentylmethylcarbonyl,cyclohexylmethylcarbonyl, cyclopropylsulphonyl, cyclobutylsulphonyl,cyclopentylsulphonyl, cyclohexylsulphonyl, cyclopropylmethylsulphonyl,cyclobutylmethylsulphonyl, cyclopentylmethylsulphonyl, orcyclohexylmethylsulphonyl; represents optionally nitro-, cyano-,fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-,i-, s-, or t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, 1-, s-,or t-butoxy-,difluoromethoxy-, trifluoromethoxy-,chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,ethoxycarbonyl-, n- or i-propoxycarbonyl-, or n-, i-, s-, ort-butoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,phenylpropyl, benzoyl, phenylacetyl, phenylsulphonyl, orphenylmethylsulphonyl; or represents optionally nitro-, cyano-,fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-,i-, s-, or t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-,or t-butoxy-, difluoromethoxy-, trifluoromethoxy-,chlorodifluoromethoxy-, fluorodichloromethoxy-, methoxycarbonyl-,ethoxycarbonyl-, n- or i-propoxycarbonyl-, or n-, i-, s-, ort-butoxycarbonyl-substituted heterocyclylcarbonyl,heterocyclylmethylcarbonyl, heterocyclylsulphonyl, orheterocyclylmethylsulphonyl, where the heterocyclyl is selected from thegroup consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diaza-cyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diaza-cyclohexyl, morpholinyl, andpiperazinyl, and R⁷ represents methoxycarbonylmethoxy,ethoxycarbonylmethoxy, n- or i-propoxycarbonylmethoxy, n-, i-, s-, ort-butoxycarbonylmethoxy, methoxycarbonylethoxy, ethoxycarbonylethoxy, n-or i-propoxycarbonylethoxy, n-, i-, s-, or t-butoxycarbonylethoxy,methoxycarbonylmethylthio, ethoxycarbonylmethylthio, n- ori-propoxycarbonylmethylthio, n-, s-, or t-butoxycarbonylmethylthio,methoxycarbonylethylthio, ethoxycarbonylethylthio, n- ori-propoxycarbonylethylthio, n-, i-, s- or t-butoxycarbonylethylthio,propenyloxycarbonylmethoxy, butenyloxycarbonylmethoxy,propenyloxycarbonylethoxy, butenyloxycarbonylethoxy,propenyloxycarbonylmethylthio, butenyloxycarbonylmethylthio,propenyloxycarbonylethylthio, butenyloxycarbonylethylthio,propynyloxycarbonylmethoxy, butynyloxycarbonylmethoxy,propynyloxycarbonylethoxy, butynyloxycarbonylethoxy,propynyloxycarbonylmethylthio, butynyloxycarbonylmethylthio,propynyloxycarbonylethylthio, butynyloxycarbonylethylthio,carbamoylmethoxy, carbamoylethoxy, carbamoylmethylthio,carbamoylethylthio, methylaminocarbonyl methoxy,ethylaminocarbonylethoxy, n- or i-propylaminocarbonylmethoxy, n-, i-,s-, or t-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-, s-,or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio, n-,i-, s-, or t-butylaminocarbonylmethylthio, methylaminocarbonylethylthio,ethylaminocarbonylethylthio, n- or i-propylaminocarbonylethylthio, n-,i-, s-, or t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio, ordipropynylaminocarbonylethylthio; represents hydroxyamino; representsN-methylhydroxyamino, N-ethylhydroxyamino, N-n-propylhydroxyamino,N-i-propylhydroxyamino, methoxyamino, ethoxyamino, n- or i-propoxyamino,n-, i-, s- or t-butoxyamino, N-methylmethoxyamino, N-ethylmethoxyamino,N-methylethoxyamino, methoxycarbonylmethoxyamino,ethoxycarbonylmethoxyamino, n- or i-propoxycarbonylmethoxyamino,methoxycarbonylethoxyamino, ethoxycarbonylethoxyamino, n- ori-propoxycarbonylethoxyamino, N-methylmethoxycarbonylmethoxyamino,N-methylethoxycarbonylmethoxyamino,N-methyl-n-propoxycarbonylmethoxyamino,N-methyl-i-propoxycarbonylmethoxyamino,N-methylmethoxycarbonylethoxyamino, N-methylethoxycarbonylethoxyamino,N-methyl-n-propoxycarbonylethoxyamino,N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,butenyloxyamino, N-methylpropenyloxyamino, N-methylbutenyloxyamino,N-propenyl-methoxyamino, N-propenylethoxyamino,N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino,N-propenylpropenyloxyamino, represents cyclopentyloxyamino,cyclohexyloxyamino, N-methylcyclopentyloxyamino, orN-methylcyclohexyloxyamino; represents phenoxyamino orN-methylphenoxyamino; represents cyanomethylamino, cyanoethylamino,cyanopropylamino, or cyanobutylamino; represents optionally cyano-,fluorine-, chlorine-, methoxy-, ethoxy-, n- or -propoxy-,methoxycarbonyl-, ethoxycarbonyl, or n- or i-propoxycarbonyl-substituteddimethylamino, diethylamino, dipropylamino, or dibutylamino; representsoptionally cyano-, fluorine-, chlorine-, methoxy-, ethoxy-, n- ori-propoxy-, methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted N-methyl-N-propenylamino,N-methyl-N-butenylamino, N-ethyl-N-propenylamino,N-ethyl-N-butenylamino, N-propyl-N-propenylamino,N-propyl-N-butenylamino, N-butyl-N-propenylamino,N-butyl-N-butenylamino, N-methyl-N-propynylamino,N-methyl-N-butynylamino, N-ethyl-N-propynylamino,N-ethyl-N-butynylamino, N-propyl-N-propynylamino,N-propyl-N-butynylamino, N-butyl-N-propynylamino, orN-butyl-N-butynylamino; represents dipropenylamino, dibutenylamino,dipropynylamino, or dibutynylamino; represents optionally nitro-,cyano-, fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- ori-propyl-, n-, i-, s-, or t-butyl-, difluoromethyl-, dichloromethyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s-, ort-butylthio-, difluoromethylthio-, trifluoromethylthio-,chlorodifluoromethylthio-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, n-, i-, s-, or t-butoxycarbonyl-,methoxycarbonylmethoxy-, acetylamino-, ethylenedioxy-, propylenedioxy-,cyclopropyl-, cyclobutyl-, cyclopentyl-, cyclohexyl-, orphenyl-substituted heterocyclyloxy, heterocyclylthio, heterocyclylamino,N-methylheterocyclylamino, N-ethylheterocyclylamino,N-methylheterocyclylmethylamino, N-ethylheterocyclylmethylamino, or—N=(heterocyclyl), where the heterocyclyl is selected from the groupconsisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl,pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl, oxazolyl,oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl, andpyrimidinyl; or represents a monocyclic or bicyclic nitrogen heterocycleselected from the group consisting of pyrrolyl, pyrrolinyl,pyrrolidinyl, oxopyrrolidinyl, pyrazolyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxo-imidazolidinyl), 2-oxooxazolidinyl,isoxazolidinyl, thiazolinyl, 2-oxothiazolidinyl, isothiazolidinyl,1-oxoisothiazolidinyl, 1,1-dioxoisothiazolidinyl,2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl, thioxotriazolinyl,pyridinyl, piperidinyl, oxopiperidinyl, 1,2-oxaza-cyclohexyl,1,2-oxazacyclohexenyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, andpiperazinyl, each of which is attached via N and is optionallysubstituted by nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl,n- or i-propyl, n-, i-, s-, or t-butyl, difluoromethyl, dichloromethyl,trifluoromethyl, chlorodifluoromethyl, fluorodichloromethyl, methoxy,ethoxy, n- or i-propoxy, n-, i-, s-, or t-butoxy, difluoromethoxy,trifluoromethoxy, chlorodifluoromethoxy, methylthio, ethylthio, n- ori-propylthio, n-, i-, s-, or t-butylthio, difluoromethylthio,trifluoromethylthio, chlorodifluoromethylthio, methoxycarbonyl,ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s-, ort-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, orphenyl.
 4. A compound of formula (I) according to claim 1 in which R¹represents hydrogen or amino; or represents optionally cyano-,fluorine-, chlorine-, methoxy-, or ethoxy-substituted methyl, ethyl, orn- or i-propyl, R² represents optionally cyano-, fluorine-, chlorine-,methoxy-, ethoxy-, or n- or i-propoxy-substituted methyl, ethyl, or n-or i-propyl, R³ represents hydrogen, fluorine, or chlorine; orrepresents optionally fluorine- or chlorine-substituted methyl or ethyl,R⁴ represents hydrogen, fluorine, or chlorine, R⁵ represents cyano,carbamoyl, thiocarbamoyl, fluorine, chlorine, or bromine; or representsoptionally fluorine- or chlorine-substituted methyl, ethyl, methoxy, orethoxy, R⁶ represents hydrogen; represents optionally cyano-, carboxyl-,fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-,ethylthio-, methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-,ethylsulphonyl-, acetyl-, propionyl-, n- or i-butyroyl-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted methyl, ethyl, n- or i-, -propyl, n-, i-,or s-butyl; represents optionally cyano-, fluorine-, chlorine-,bromine-, methoxy-, ethoxy-, or n- or i-propoxy-substituted acetyl,propionyl, n- or i-butyroyl, methoxycarbonyl, ethoxycarbonyl, n- ori-propoxycarbonyl, methylsulphonyl, ethylsulphonyl, n- ori-propylsulphonyl, or n-, i-, or s-butylsulphonyl; represents optionallyfluorine-, chlorine-, or bromine-substituted propenyl, butenyl,propynyl, or butynyl; represents optionally cyano-, fluorine-,chlorine-, methyl-, or ethyl-substituted cyclopropyl, cyclopentyl,cyclohexyl, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl,cyclopropylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl,cyclopropylsulphonyl, cyclopentylsulphonyl, or cyclohexylsulphonyl;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-, or n-, i-,s-, or t-butoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl;and R⁷ represents methoxycarbonylmethoxy, ethoxycarbonylmethoxy, n- ori-propoxycarbonylmethoxy, n-, i-, s-, or t-butoxycarbonylmethoxy,methoxycarbonylethoxy, ethoxycarbonylethoxy, n- ori-propoxycarbonylethoxy, n-, i-, s-, or t-butoxycarbonylethoxy,methoxycarbonylmethylthio, ethoxycarbonylmethylthio, n- ori-propoxycarbonylmethylthio, n-, i-, s-, or t-butoxycarbonylmethylthio,methoxycarbonylethylthio, ethoxycarbonylethylthio, n- ori-propoxycarbonylethylthio, n-, i-, s-, or t-butoxycarbonylethylthio,propenyloxycarbonylmethoxy, butenyloxycarbonylmethoxy,propenyloxycarbonylethoxy, butenyloxycarbonylethoxy, propenyloxycarbonylmethylthio, butenyloxycarbonylmethylthio, propenyloxycarbonylethylthio,butenyloxycarbonylethylthio, propynyloxycarbonylmethoxy,butynyloxycarbonylmethoxy, propynyloxycarbonylethoxy,butynyloxycarbonylethoxy, propynyloxycarbonylmethylthio,butynyloxycarbonylmethylthio, propynyloxycarbonylethylthio,butynyloxycarbonylethylthio, methylaminocarbonylmethoxy,ethylaminocarbonylethoxy, n- or i-propylaminocarbonylmethoxy, n-, i-,s-, or t-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-, s-,or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio, n-,i-, s-, or t-butylaminocarbonylmethylthio, methylaminocarbonylethylthio,ethylaminocarbonylethylthio, n- or i-propylaminocarbonylethylthio, n-,i-, s-, or t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio, ordipropynylaminocarbonylethylthio; represents hydroxyamino; representsN-methylhydroxyamino, N-ethyl-hydroxyamino, N-n-propylhydroxyamino,N-i-propylhydroxyamino, methoxyamino, ethoxyamino, n- or i-propoxyamino,n-, i-, s-, or t-butoxyamino, N-methylmethoxyamino, N-ethylmethoxyamino,N-methylethoxyamino, methoxycarbonylmethoxyamino,ethoxycarbonylmethoxyamino, n- or i-propoxycarbonylmethoxyamino,methoxycarbonylethoxyamino, ethoxycarbonylethoxyamino, n- ori-propoxycarbonylethoxyamino, N-methylmethoxycarbonylmethoxyamino,N-methylethoxycarbonylmethoxyamino,N-methyl-n-propoxycarbonylmethoxyamino,N-methyl-i-propoxycarbonylmethoxyamino,N-methyl-methoxycarbonylethoxyamino, N-methylethoxycarbonylethoxyamino,N-methyl-n-propoxycarbonylethoxyamino,N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,butenyloxyamino, N-methylpropenyloxyamino, N-methylbutenyloxyamino,N-propenylmethoxyamino, N-propenylethoxyamino,N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino,N-propenylpropenyloxyamino; represents phenoxyamino orN-methylphenoxyamino; represents cyanoethylamino, cyanopropylamino, orcyanobutylamino; represents dimethylamino, diethylamino,di-n-propylamino, di-i-propylamino, di-n-butylamino, or di-i-butylamino;represents N-methylcyanoethylamino, N-ethylcyanoethylamino,N-n-propylcyanoethylamino, N-i-propylcyanoethylamino,N-methylfluoroethylamino, N-ethylfluoroethylamino,N-n-propylfluoroethylamino, N-i-propylfluoroethylamino,N-methylmethoxyethylamino, N-ethylmethoxyethylamino,N-methylethoxyethylamino, N-ethylethoxyethylamino,N-methylmethoxycarbonylmethylamino, N-methylethoxycarbonylmethylamino,N-methylmethoxycarbonylethylamino, N-methylethoxycarbonylethylamino,represents N-methyl-N-propenylamino, N-methyl-N-butenylamino,N-ethyl-N-propenylamino, N-ethyl-N-butenylamino,N-propyl-N-propenylamino, N-propyl-N-butenylamino,N-butyl-N-propenylamino, N-butyl-N-butenylamino,N-methyl-N-propynylamino, N-methyl-N-butynylamino,N-ethyl-N-propynylamino, N-ethyl-N-butynylamino,N-propyl-N-propynylamino, N-propyl-N-butynylamino,N-butyl-N-propynylamino, or N-butyl-N-butynylamino; representsdipropenylamino, dibutenylamino, dipropynylamino, or dibutynylamino;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,difluoromethyl-, dichloromethyl-, trifluoromethyl-,chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n- ori-propoxy-, n-, i-, s-, or t-butoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, methylthio-, ethylthio-, n-or i-propylthio-, n-, i-, s-, or t-butylthio-, difluoromethylthio-,trifluoromethylthio-, chlorodifluoromethylthio-, methoxycarbonyl-,ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, i-, s-, ort-butoxycarbonyl-, cyclopropyl-, cyclobutyl-, cyclopentyl-, cyclohexyl-,or phenyl-substituted heterocyclyloxy, heterocyclylthio,heterocyclylamino, N-methylheterocyclylamino,N-methylheterocyclylmethylamino, or —N=(heterocyclyl), where theheterocyclyl is selected from the group consisting of furyl,tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl,oxopyrrolidinyl, pyrrolyl, pyrazolyl, oxazolyl, oxazolinyl,oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl, thiazolidinyl,cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl, andpyrimidinyl; represents a monocyclic or bicyclic nitrogen heterocycleselected from the group consisting of pyrrolyl, pyrrolinyl,pyrrolidinyl, oxopyrrolidinyl, pyrazolyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxo-imidazolidinyl), 2-oxo-1,3-oxazacyclopentyl (2-oxooxazolidinyl), isoxazolidinyl, thiazolinyl,2-oxothiazolidinyl, 1,1-dioxoisothiazolidinyl,2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl, thioxotriazolinyl,pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,morpholinyl, and piperazinyl, each of which is attached via N and isoptionally substituted by nitro, cyano, fluorine, chlorine, bromine,methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, difluoromethyl,dichloromethyl, trifluoromethyl, chlorodifluoromethyl,fluorodichloromethyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s-, ort-butoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy,methylthio, ethylthio, n- or i-propylthio, n-, i-, s-, or t-butylthio,difluoromethylthio, trifluoromethylthio, chlorodifluoromethylthio,methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s-, ort-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, orphenyl.
 5. A compound of formula (I) according to claim 1 in which R⁶represents hydrogen; or represents optionally fluorine-, chlorine-,methoxy-, or ethoxy-substituted methyl, ethyl, acetyl, methoxycarbonyl,or ethoxycarbonyl.
 6. A compound of formula (I) according to claim 1 inwhich Q represents oxygen, R¹ represents hydrogen, amino, or methyl, R²represents cyano or trifluoromethyl, R³ represents hydrogen, chlorine,or methyl, R⁴ represents hydrogen, fluorine, or chlorine, R⁵ representscyano, thiocarbamoyl, chlorine, bromine, or trifluoromethyl, R⁶represents hydrogen; represents optionally cyano-, fluorine-, chlorine-,methoxy-, ethoxy-, methylthio-, ethylthio-, methylsulphinyl-,ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, acetyl-, propionyl-,methoxycarbonyl-, or ethoxycarbonyl-substituted methyl or ethyl;represents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,or ethoxy-substituted acetyl, propionyl, methoxycarbonyl, orethoxycarbonyl; represents optionally fluorine- or chlorine-substitutedmethylsulphonyl or ethylsulphonyl; represents optionally fluorine- orchlorine-substituted propenyl, butenyl, propynyl, or butynyl; representsoptionally fluorine-, chlorine-, or methyl-substituted cyclopropyl,cyclopropylmethyl, cyclopropylcarbonyl, or cyclopropylsulphonyl;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl,and R⁷ represents methoxycarbonylmethoxy, ethoxycarbonylmethoxy, n- ori-propoxycarbonylmethoxy, n-, i-, s-, or t-butoxycarbonylmethoxy,methoxycarbonylethoxy, ethoxycarbonylethoxy, n- ori-propoxycarbonylethoxy, n-, i-, s-, or t-butoxycarbonylethoxy,methoxycarbonylmethylthio, ethoxycarbonylmethylthio, n- ori-propoxycarbonylmethylthio, n-, i-, s-, or t-butoxycarbonyl-methylthio,methoxycarbonylethylthio, ethoxycarbonylethylthio, n- ori-propoxycarbonylethylthio, n-, i-, s-, or t-butoxycarbonylethylthio,propenyloxycarbonylmethoxy, butenyloxycarbonylmethoxy,propenyloxycarbonylethoxy, butenyloxycarbonylethoxy,propenyloxycarbonylmethylthio, butenyloxycarbonylmethylthio,propenyloxycarbonylethylthio, butenyloxycarbonylethylthio,propynyloxycarbonylmethoxy, butynyloxycarbonylmethoxy,propynyloxycarbonylethoxy, butynyloxycarbonylethoxy,propynyloxycarbonylmethylthio, butynyloxycarbonylmethylthio,propynyloxycarbonylethylthio, butynyloxycarbonylethylthio,methylaminocarbonylmethoxy, ethylaminocarbonylethoxy, n- ori-propylaminocarbonylmethoxy, n-, i-, s-, ort-butylaminocarbonylmethoxy, methylaminocarbonylethoxy,ethylaminocarbonylethoxy, n- or i-propylaminocarbonylethoxy, n-, i-, s-or t-butylaminocarbonylethoxy, methylaminocarbonylmethylthio,ethylaminocarbonylmethylthio, n- or i-propylaminocarbonylmethylthio, n-,i-, s-, or t-butylaminocarbonylmethylthio, methylaminocarbonylethylthio,ethylaminocarbonylethylthio, n- or i-propylaminocarbonylethylthio, n-,i-, s-, or t-butylaminocarbonylethylthio, dimethylaminocarbonylmethoxy,diethylaminocarbonylmethoxy, dimethylaminocarbonylethoxy,diethylaminocarbonylethoxy, dimethylaminocarbonylmethylthio,diethylaminocarbonylmethylthio, dimethylaminocarbonylethylthio,diethylaminocarbonylethylthio, dipropenylaminocarbonylmethoxy,dipropenylaminocarbonylethoxy, dipropenylaminocarbonylmethylthio,dipropenylaminocarbonylethylthio, dipropynylaminocarbonylmethoxy,dipropynylaminocarbonylethoxy, dipropynylaminocarbonylmethylthio, ordipropynylaminocarbonylethylthio.
 7. A compound of formula (I) accordingto claim 1 in which Q represents oxygen, R¹ represents hydrogen, amino,or methyl, R² represents cyano or trifluoromethyl, R³ representshydrogen, chlorine, or methyl, R⁴ represents hydrogen, fluorine, orchlorine, R⁵ represents cyano, thiocarbamoyl, chlorine, bromine, ortrifluoromethyl, R⁶ represents hydrogen; represents optionally cyano-,fluorine-, chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-,methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-,acetyl-, propionyl-, methoxycarbonyl-, or ethoxycarbonyl-substitutedmethyl or ethyl; represents optionally cyano-, fluorine-, chlorine-,bromine-, methoxy-, or ethoxy-substituted acetyl, propionyl,methoxycarbonyl, or ethoxycarbonyl; represents optionally fluorine- orchlorine-substituted methylsulphonyl or ethylsulphonyl; representsoptionally fluorine- or chlorine-substituted propenyl, butenyl,propynyl, or butynyl; represents optionally fluorine-, chlorine-, ormethyl-substituted cyclopropyl, cyclopropylmethyl, cyclopropylcarbonyl,or cyclopropylsulphonyl; represents optionally nitro-, cyano-,fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-,i-, s-, or t-butyl-, trifluoromethyl-, chlorodifluoromethyl-,fluorodichloromethyl-, methoxy-, ethoxy-, n- or i-propoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl,and R⁷ represents hydroxyamino; represents N-methylhydroxyamino,N-ethylhydroxyamino, N-n-propylhydroxyamino, N-i-propylhydroxyamino,methoxyamino, ethoxyamino, n- or i-propoxyamino, n-, i-, s-, ort-butoxyamino, N-methylmethoxyamino, N-ethylmethoxyamino,N-methylethoxyamino, methoxycarbonylmethoxyamino,ethoxycarbonylmethoxyamino, n- or i-propoxycarbonylethoxyamino,methoxycarbonylethoxyamino, ethoxycarbonylethoxyamino, n- ori-propoxycarbonylethoxyamino, N-methylmethoxycarbonylmethoxyamino,N-methylethoxycarbonylmethoxyamino,N-methyl-n-propoxycarbonylmethoxyamino,N-methyl-i-propoxycarbonylmethoxyamino,N-methylmethoxycarbonylethoxyamino, N-methylethoxycarbonylethoxyamino,N-methyl-n-propoxycarbonylethoxyamino,N-methyl-i-propoxycarbonylethoxyamino, propenyloxyamino,butenyloxyamino, N-methylpropenyloxyamino, N-methylbutenyloxyamino,N-propenylmethoxyamino, N-propenylethoxyamino,N-propenyl-n-propoxyamino, N-propenyl-i-propoxyamino, orN-propenylpropenyloxyamino; or represents phenoxyamino orN-methylphenoxyamino.
 8. A compound of formula (I) according to claim 1in which Q represents oxygen, R¹ represents hydrogen, amino, or methyl,R² represents cyano or trifluoromethyl, R³ represents hydrogen,chlorine, or methyl, R⁴ represents hydrogen, fluorine, or chlorine, R⁵represents cyano, thiocarbamoyl, chlorine, bromine, or trifluoromethyl,R⁶ represents hydrogen; represents optionally cyano-, fluorine-,chlorine-, methoxy-, ethoxy-, methylthio-, ethylthio-, methylsulphinyl-,ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, acetyl-, propionyl-,methoxycarbonyl-, or ethoxycarbonyl-substituted methyl or ethyl;represents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,or ethoxy-substituted acetyl, propionyl, methoxycarbonyl, orethoxycarbonyl; represents optionally fluorine- or chlorine-substitutedmethylsulphonyl or ethylsulphonyl; represents optionally fluorine- orchlorine-substituted propenyl, butenyl, propynyl, or butynyl; representsoptionally fluorine-, chlorine-, or methyl-substituted cyclopropyl,cyclopropylmethyl, cyclopropylcarbonyl, or cyclopropylsulphonyl;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diaza-cyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl,and R⁷ represents cyanoethylamino, cyanopropylamino, or cyanobutylamino;represents dimethylamino, diethylamino, di-n-propylamino,di-i-propylamino, di-n-butylamino, or di-i-butylamino; representsN-methylcyanoethylamino, N-ethylcyanoethylamino,N-n-propylcyanoethylamino, N-i-propylcyanoethylamino,N-methylfluoroethylamino, N-ethylfluoroethylamino,N-n-propylfluoroethylamino, N-i-propylfluoroethylamino,N-methylmethoxyethylamino, N-ethylmethoxyethylamino,N-methylethoxyethylamino, N-ethylethoxyethylamino,N-methylmethoxycarbonylmethylamino, N-methylethoxycarbonylmethylamino,N-methylmethoxycarbonylethylamino, N-methylethoxycarbonylethylamino,represents N-methyl-N-propenylamino, N-methyl-N-butenylamino,N-ethyl-N-propenylamino, N-ethyl-N-butenylamino,N-propyl-N-propenylamino, N-propyl-N-butenylamino,N-butyl-N-propenylamino, N-butyl-N-butenylamino,N-methyl-N-propynylamino, N-methyl-N-butynylamino,N-ethyl-N-propynylamino, N-ethyl-N-butynylamino,N-propyl-N-propynylamino, N-propyl-N-butynylamino,N-butyl-N-propynylamino, or N-butyl-N-butynylamino; or representsdipropenylamino, dibutenylamino, dipropynylamino, or dibutynylamino. 9.A compound of formula (I) according to claim 1 in which Q representsoxygen, R¹ represents hydrogen, amino, or methyl, R² represents cyano ortrifluoromethyl, R³ represents hydrogen, chlorine, or methyl, R⁴represents hydrogen, fluorine, or chlorine, R⁵ represents cyano,thiocarbamoyl, chlorine, bromine, or trifluoromethyl, R⁶ representshydrogen; represents optionally cyano-, fluorine-, chlorine-, methoxy-,ethoxy-, methylthio-, ethylthio-, methylsulphinyl-, ethylsulphinyl-,methylsulphonyl-, ethylsulphonyl-, acetyl-, propionyl-,methoxycarbonyl-, or ethoxycarbonyl-substituted methyl or ethyl;represents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,or ethoxy-substituted acetyl, propionyl, methoxycarbonyl, orethoxycarbonyl; represents optionally fluorine- or chlorine-substitutedmethylsulphonyl or ethylsulphonyl; represents optionally fluorine- orchlorine-substituted propenyl, butenyl, propynyl, or butynyl; representsoptionally fluorine-, chlorine-, or methyl-substituted cyclopropyl,cyclopropylmethyl, cyclopropylcarbonyl, or cyclopropylsulphonyl;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl,and R⁷ represents optionally nitro-, cyano-, fluorine-, chlorine-,bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,difluoromethyl-, dichloromethyl-, trifluoromethyl-,chlorodifluoromethyl-, fluorodichloromethyl-, methoxy-, ethoxy-, n- ori-propoxy-, n-, i-, s-, or t-butoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, methylthio-, ethylthio-, n-or i-propylthio-, n-, i-, s-, or t-butylthio-, difluoromethylthio-,trifluoromethylthio-, chlorodifluoromethylthio-, methoxycarbonyl-,ethoxycarbonyl-, n- or i-propoxycarbonyl-, n-, s-, or t-butoxycarbonyl-,cyclopropyl-, cyclobutyl-, cyclopentyl-, cyclohexyl-, orphenyl-substituted heterocyclyloxy, heterocyclylthio, heterocyclylamino,N-methylheterocyclylamino, N-methylheterocyclylmethylamino, or—N=(heterocyclyl), where the heterocyclyl is selected from the groupconsisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl,pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl, oxazolyl,oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, piperazinyl, andpyrimidinyl.
 10. A compound of formula (I) according to claim 1 in whichQ represents oxygen, R¹ represents hydrogen, amino, or methyl, R²represents cyano or trifluoromethyl, R³ represents hydrogen, chlorine,or methyl, R⁴ represents hydrogen, fluorine, or chlorine, R⁵ representscyano, thiocarbamoyl, chlorine, bromine, or trifluoromethyl, R⁶represents hydrogen; represents optionally cyano-, fluorine-, chlorine-,methoxy-, ethoxy-, methylthio-, ethylthio-, methylsulphinyl-,ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, acetyl-, propionyl-,methoxycarbonyl-, or ethoxycarbonyl-substituted methyl or ethyl;represents optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-,or ethoxy-substituted acetyl, propionyl, methoxycarbonyl, orethoxycarbonyl; represents optionally fluorine- or chlorine-substitutedmethylsulphonyl or ethylsulphonyl; represents optionally fluorine- orchlorine-substituted propenyl, butenyl, propynyl, or butynyl; representsoptionally fluorine-, chlorine-, or methyl-substituted cyclopropyl,cyclopropylmethyl, cyclopropylcarbonyl, or cyclopropylsulphonyl;represents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-,trifluoromethoxy-, chlorodifluoromethoxy-, fluorodichloromethoxy-,methoxycarbonyl-, ethoxycarbonyl-, or n- ori-propoxycarbonyl-substituted phenyl, phenylmethyl, phenylethyl,benzoyl, phenylacetyl, phenylsulphonyl, or phenylmethylsulphonyl; orrepresents optionally nitro-, cyano-, fluorine-, chlorine-, bromine-,methyl-, ethyl-, n- or i-propyl-, n-, i-, s-, or t-butyl-,trifluoromethyl-, chlorodifluoromethyl-, fluorodichloromethyl-,methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s-, or t-butoxy-,difluoromethoxy-, trifluoromethoxy-, chlorodifluoromethoxy-,fluorodichloromethoxy-, methoxycarbonyl-, ethoxycarbonyl-, n- ori-propoxycarbonyl-, or n-, i-, s-, or t-butoxycarbonyl-substitutedheterocyclylcarbonyl, heterocyclylmethylcarbonyl, heterocyclylsulphonyl,or heterocyclylmethylsulphonyl, where the heterocyclyl is selected fromthe group consisting of furyl, tetrahydrofuryl, thienyl, pyrrolyl,pyrrolinyl, pyrrolidinyl, oxopyrrolidinyl, pyrrolyl, pyrazolyl,oxazolyl, oxazolinyl, oxazolidinyl, isoxazolyl, thiazolyl, thiazolinyl,thiazolidinyl, cyanoiminothiazolidinyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxoimidazolidinyl), triazolyl,oxotriazolinyl, thioxotriazolinyl, pyridinyl, piperidinyl,oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl, morpholinyl, and piperazinyl,and R⁷ represents a monocyclic or bicyclic nitrogen heterocycle selectedfrom the group consisting of pyrrolyl, pyrrolinyl, pyrrolidinyl,oxopyrrolidinyl, pyrazolyl, imidazolyl, imidazolinyl,2-oxo-1,3-diazacyclopentyl (2-oxo-imidazolidinyl),2-oxo-1,3-oxazacyclopentyl (2-oxooxazolidinyl), isoxazolidinyl,thiazolinyl, 2-oxothiazolidinyl, 1,1-dioxoisothiazolidinyl,2-cyanoiminothiazolidinyl, triazolyl, oxotriazolinyl, thioxotriazolinyl,pyridinyl, piperidinyl, oxopiperidinyl, 2-oxo-1,3-diazacyclohexyl,morpholinyl, and piperazinyl, each of which is attached via N and isoptionally substituted by nitro, cyano, fluorine, chlorine, bromine,methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, difluoromethyl,dichloromethyl, trifluoromethyl, chlorodifluoromethyl,fluorodichloromethyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s-, ort-butoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy,methylthio, ethylthio, n- or i-propylthio, n-, i-, s-, or t-butylthio,difluoromethylthio, trifluoromethylthio, chlorodifluoromethylthio,methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, n-, i-, s-, ort-butoxycarbonyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, orphenyl.
 11. A process for preparing compounds of formula (I) accordingto claim 1 comprising (a) reacting a compound of formula (II)

in which Q, R¹, R², R³, R⁴, and R⁵ are as defined for formula (I) inclaim 1, with a compound of formula (III)H—R⁷  (III) in which R⁷ is as defined for formula (I) in claim 1,optionally in the presence of one or more reaction auxiliaries andoptionally in the presence of one or more diluents, to form a compoundof formula (Ia)

in which Q, R¹, R², R³, R⁴, R⁵, and R⁷ are as defined for formula (I) inclaim 1, and (b) optionally reacting the compound of formula (Ia) with acompound of formula (IV)X—R⁶  (IV) in which R⁶ is as defined as for formula (I) in claim 1 butis not hydrogen, and X represents halogen or represents acetyloxy,propionyloxy, methoxysulphonyloxy, or ethoxysulphonyloxy, optionally inthe presence of one or more reaction auxiliaries and optionally in thepresence of one or more diluents.
 12. A compound of formula (II)

in which Q represents oxygen, R¹ represents hydrogen or amino; orrepresents optionally cyano-, halogen-, or C₁-C₄-alkoxy-substitutedalkyl having 1 to 6 carbon atoms, R² represents carboxyl, cyano,carbamoyl, or thiocarbamoyl; or represents optionally cyano-, halogen-,or C₁-C₄-alkoxy-substituted alkyl or alkoxycarbonyl having in each case1 to 6 carbon atoms in the alkyl groups, R³ represents hydrogen orhalogen; or represents optionally halogen-substituted alkyl having 1 to6 carbon atoms, R⁴ represents hydrogen, cyano, carbamoyl, thiocarbamoyl,or halogen, and R⁵ represents cyano, carbamoyl, thiocarbamoyl, orhalogen; or represents optionally halogen-substituted alkyl or alkoxyhaving in each case 1 to 6 carbon atoms.
 13. A composition comprisingone or more compounds of formula (I) according to claim 1 and one ormore extenders and/or surfactants.
 14. A method for controlling unwantedplants comprising allowing an effective amount of a compound of formula(I) according to claim 1 to act on the plant and/or its habitat.
 15. Amethod for controlling unwanted plants comprising allowing an effectiveamount of a composition according to claim 13 to act on the plant and/orits habitat.